Recall events
/
Event 84688
Event summary
Timeline bucket December 20, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Arrow International 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
20 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 20
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
Z-1236-2020
Recall number Z-1236-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 250 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1236-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27363]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0527
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[12161]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 20
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
Z-1237-2020
Recall number Z-1237-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1237-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44640]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18B0063
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11766]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 20
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
Z-1238-2020
Recall number Z-1238-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 205
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1238-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50442]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18K0740
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[12135]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 20
Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
Z-1239-2020
Recall number Z-1239-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 1150 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1239-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44638]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0714
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11217]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 20
Arrow Maximal Barrier Drape ASK-00002-1A
Z-1240-2020
Recall number Z-1240-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 2080
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1240-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21645]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18G0481 13F18H0652 13F18K0645
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[9670]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 20
Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
Z-1241-2020
Recall number Z-1241-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 155
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1241-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57107]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0547
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[8514]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 20
Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM
Z-1242-2020
Recall number Z-1242-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 410
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1242-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11250]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18G0475 13F18F0729
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11207]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 20
Arrow Central Venous Catheterization Kit ASK-04200-UPM
Z-1243-2020
Recall number Z-1243-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 140
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1243-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11248]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18H0209
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[13258]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 20
Arrow EPIDURAL NEEDLE COMPONENT AN-05505
Z-1244-2020
Recall number Z-1244-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 1839
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1244-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21638]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18H0836 13F17L0441 13R17L0441
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[13222]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1245-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 870
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1245-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11247]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0451
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[12119]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1246-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 160
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1246-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44635]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0593
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11257]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1247-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 1760
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1247-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44646]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0719
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[12122]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1248-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 1320
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1248-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57109]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0745
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[8453]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1249-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 1360
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1249-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44636]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0713 13F18B0394
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[8459]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1250-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 90
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1250-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50447]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot number13F18A0715:
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[13235]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1251-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 540
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1251-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21640]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18D0313
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11202]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1252-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 180
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1252-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33207]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F17H0053
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[11197]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1253-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity 2126
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1253-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44648]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: (1) AB-00150 13F16B0155; (2) AB-17080-N 13F18J0654, 13F16H0046,13F16F0210, 13F16E0106, 13F16C0107; (3) AB-17110-N 13F16G0226, 13R16G0226, 13F16F0079; (4) AB-17140-N 13F16F0190, 13F16C0045; (5) AB-18080-N 13F16H0048, 13F16F0007, 13F16B0181, (6) AB-18110-N 13F16F0189, 13F16C0046; (7) AB-18140-N 13F16H0292;
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[8456]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1254-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1254-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38743]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18A0540
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[12163]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1255-2020
Initiated December 20, 2019
Classification Class II
Status Terminated
Quantity Unavailable
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lidstock contains the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Incorrect or no expiration date
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1255-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38745]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lidstock contains the incorrect expiration date for the product
Code information Lot Number: 13F18G0925
Distribution pattern Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
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[9352]
FDA event record
· Exact recall-number query on openFDA
