Recall events
/
Event 67665
Event summary
Timeline bucket March 04, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording LumiQuick Diagnostics Inc.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
80 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 80
Syphilis Test Strip (Serum) LumiQuick, Santa Clara, CA 95054
Z-1337-2014
Recall number Z-1337-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1337-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17841]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71015, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17312]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 80
Syphilis Test Card Whole Blood(Serum) LumiQuick, Santa Clara, CA 95054
Z-1338-2014
Recall number Z-1338-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1338-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47229]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71016, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22015]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 80
Rickettsia IgG/IgM Test Card LumiQuick, Santa Clara, CA 95054
Z-1339-2014
Recall number Z-1339-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1339-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53081]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71017, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20210]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 80
Dengue IgG/IgM; LumiQuick, Santa Clara, CA 95054
Z-1340-2014
Recall number Z-1340-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1340-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23626]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71019, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20299]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 80
H. Pylori Antigen Test Card LumiQuick, Santa Clara, CA 95054
Z-1341-2014
Recall number Z-1341-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1341-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47230]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71020, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20291]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 80
H. Pylori Antibody Test Card (Whole Blood) LumiQuick, Santa Clara, CA 95054
Z-1342-2014
Recall number Z-1342-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1342-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6074]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71024, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16840]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 80
Salmonella typhi Antigen Test Card; LumiQuick, Santa Clara, CA 95054
Z-1343-2014
Recall number Z-1343-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1343-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41311]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71028, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16093]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 80
Rotavirus Test Card LumiQuick, Santa Clara, CA 95054
Z-1344-2014
Recall number Z-1344-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1344-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[125]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71029, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16135]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 80
Adenovirus Antigen Test Card; LumiQuick, Santa Clara, CA 95054
Z-1345-2014
Recall number Z-1345-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1345-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23629]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71032, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20142]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1346-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1346-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11940]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71033, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20215]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1347-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1347-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11943]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71034, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22376]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1348-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1348-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6077]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71046, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22521]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1349-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1349-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29614]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71048, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22536]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1350-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1350-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11946]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71049, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17276]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1351-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1351-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29618]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71050, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22517]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1352-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1352-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6080]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71053, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20335]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1353-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1353-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41307]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71054, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22408]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1354-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1354-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[120]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71055, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22525]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1355-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1355-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29610]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71057, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20321]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1356-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1356-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53085]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71062, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20255]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1357-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1357-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17836]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71063, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20294]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1358-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1358-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17843]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71066, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17100]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1359-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1359-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6078]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 71087, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16080]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1360-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1360-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47231]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 72001, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20199]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1361-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1361-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11941]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 72003, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20284]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1362-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1362-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47233]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 72004, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16125]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1363-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1363-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[121]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 72006, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20224]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1364-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1364-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[123]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74001, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20193]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1365-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1365-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53082]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74002, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20179]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1366-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1366-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[119]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74003, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16089]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1367-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1367-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53083]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74007, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22403]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1368-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1368-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17835]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74013, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20241]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1369-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1369-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6073]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74014, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20277]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1370-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1370-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35365]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74015, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20236]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1371-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1371-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53084]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74016, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16845]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1372-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1372-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35368]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74017, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22363]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1373-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1373-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35367]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74018, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17074]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1374-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1374-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53080]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74019, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20296]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1375-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1375-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6076]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74020, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22366]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1376-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1376-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29617]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74021, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20285]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1377-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1377-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17838]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74022, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16816]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1378-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1378-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11944]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74023, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16849]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1379-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1379-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23627]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74024, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17303]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1380-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1380-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[126]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74025, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22555]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1381-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1381-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6079]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74026, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17268]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1382-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1382-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47226]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74027, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20316]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1383-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1383-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17840]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74028, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17044]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1384-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1384-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47234]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74029, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16110]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1385-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1385-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29615]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74030, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16831]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1386-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1386-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17842]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74031, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20228]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1387-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1387-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[122]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74032, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17070]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1388-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1388-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47227]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74033, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17317]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1389-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1389-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29613]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74034, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22397]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1390-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1390-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11942]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74035 All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16862]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1391-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1391-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29612]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74036 All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16098]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1392-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1392-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47235]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74039 All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16067]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1393-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1393-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23625]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74040 All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17278]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1394-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1394-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[53079]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74041 All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17060]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1395-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1395-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41309]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74042, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17306]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1396-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1396-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6082]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74043, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16819]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1397-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1397-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17839]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74044, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22050]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1398-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1398-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41308]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74049, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16867]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1399-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1399-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23628]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74051, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20170]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1400-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1400-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41312]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74052, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22011]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1401-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1401-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6081]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74055, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16078]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1402-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1402-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35366]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74056, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17053]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1403-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1403-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29616]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74057, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17078]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1404-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1404-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17837]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74058, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20253]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1405-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1405-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47236]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74059, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16857]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1406-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1406-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29611]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74060, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17282]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1407-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1407-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35369]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74065, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20308]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1408-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1408-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47232]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 74066, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22026]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1409-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1409-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11945]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75001, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22390]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1410-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1410-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[124]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75002, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20324]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1411-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1411-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[47228]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75003, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20327]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1412-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1412-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[6075]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75004, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[17110]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1413-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1413-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[118]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75005, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22420]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1414-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1414-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41310]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75006, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20196]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1415-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1415-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[35364]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75007, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[22388]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1416-2014
Initiated March 04, 2014
Classification Class II
Status Terminated
Quantity ALL
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1416-2014
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23624]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Code information Catalog number: 75008, All lots
Distribution pattern Distributed in the states of CA, FL, NJ, TX, and NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[16142]
FDA event record
· Exact recall-number query on openFDA
