Recall events
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Event 98895
Event summary
Timeline bucket April 30, 2026
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording CareFusion 303, 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
8 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 8
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Z-2297-2026
Recall number Z-2297-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2297-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23507]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403512629
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[347]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 8
BD Pyxis MedStation ES REF: 323 Medication cabinet
Z-2298-2026
Recall number Z-2298-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 15,933
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2298-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46789]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403512667
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[279]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 8
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Z-2299-2026
Recall number Z-2299-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 4,579 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2299-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41171]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403477836
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[359]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 8
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Z-2300-2026
Recall number Z-2300-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2300-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29474]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403477829
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[348]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 8
BD Pyxis Mini Main REF: 349 Medication cabinet
Z-2301-2026
Recall number Z-2301-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 709 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2301-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[41166]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403512582
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[326]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 8
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Z-2302-2026
Recall number Z-2302-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 465 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2302-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5932]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403512674
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[368]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 8
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Z-2303-2026
Recall number Z-2303-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 607 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2303-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29476]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403517167
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[361]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 8
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Z-2304-2026
Recall number Z-2304-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 114 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Component design/selection
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2304-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29473]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Code information All Serial Numbers/UDI:10885403517181
Distribution pattern US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
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[336]
FDA event record
· Exact recall-number query on openFDA
