Pyxis recallZ-2297-2026 · CareFusion 303, Inc. · initiated Apr 30, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from CareFusion 303, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
FDA root cause category: Component design/selection
What the company is doing
On April 30, 2026, CareFusion (subsidiary of Becton, Dickinson and Company) issued a Urgent Medical Device Recall Notification, via mail or Email. CareFusion ask consignees to take the following actions: 1. Dispensing cabinets can continue to be used as intended. 2. If you suspect that the Bio-ID Scanner is hot, please discontinue the use of Scanner and file a complaint. 3. Review and update facility policies and procedures related to situations where the Bio-ID Scanner is unavailable to mitigate delays in care. 4. Complete the attached Customer Response Form and return to the BD contact noted on the form.
Recall details
- Recall number
- Z-2297-2026
- Status
- Open, Classified
- Initiated by the company
- Apr 30, 2026
- Posted by the FDA
- Jun 3, 2026
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 1 unit
- Product code
- BRY
- Distribution
- US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Product description
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Code information (models, lots, serial numbers)
All Serial Numbers/UDI:10885403512629
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Pyxis 303Carefusion 303, Inc. · CABINET, TABLE AND TRAY, ANESTHESIA7 recalls392 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 98895).
- Z-2298-2026 · Open, ClassifiedBD Pyxis MedStation ES REF: 323 Medication cabinet
- Z-2299-2026 · Open, ClassifiedBD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
- Z-2300-2026 · Open, ClassifiedBD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
- Z-2301-2026 · Open, ClassifiedBD Pyxis Mini Main REF: 349 Medication cabinet
- Z-2302-2026 · Open, ClassifiedBD Pyxis MedStation ES Tower REF: 352 Medication cabinet
- Z-2303-2026 · Open, ClassifiedBD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
- Z-2304-2026 · Open, ClassifiedBD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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