Recall events
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Event 90658
Event summary
Timeline bucket July 22, 2022
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Baxter Healthcare Corporation
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
7 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 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H938690025
Z-1575-2022
Recall number Z-1575-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 602340 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1575-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33628]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information a) REF H93866025, UDI 00085412478845, ALL LOTS; b) REF H93866100, UDI 00085412478852, ALL LOTS; c) REF H938690025, UDI 00085412479941, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7168]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100
Z-1576-2022
Recall number Z-1576-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 63190 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1576-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51817]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information a) REF H93867025, UDI 00085412478869, ALL LOTS; b) REF H93867100, UDI 00085412478890, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7177]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100
Z-1577-2022
Recall number Z-1577-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 10140 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1577-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4506]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information REF H938671100, UDI 00085412479750
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7057]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF H938693025, b) 100 pack REF H938673100
Z-1578-2022
Recall number Z-1578-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 24,320 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1578-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16600]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information a) 25 pack REF H938693025, UDI 00085412479965, ALL LOTS; b) 100 pack REF H938673100, UDI 00085412479798, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7082]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
Z-1579-2022
Recall number Z-1579-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 168390 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1579-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4494]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information a) 25 pack, REF H93869025, UDI 00085412479965, ALL LOTS; b) 100 pack, REF H938674100, UDI 00085412479811, ALL LOTS; c) 100 pack, REF H93869100, UDI 00085412478944, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7138]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100
Z-1580-2022
Recall number Z-1580-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 9700 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1580-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45384]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information REF H938676100, UDI 00085412479859, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7174]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 7
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
Z-1581-2022
Recall number Z-1581-2022
Initiated July 22, 2022
Classification Class II
Status Ongoing
Quantity 8500 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1581-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51821]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Code information REF H938677100 , UDI 00085412479873, ALL LOTS
Distribution pattern Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
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[7001]
FDA event record
· Exact recall-number query on openFDA
