BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
FDA device recall Z-2300-2026 · posted 2026-06-03 · Open, Classified
Recall details
- Recalling firm
- CareFusion 303, Inc.
- Reason for recall
- Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Action taken
- 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.
- Root cause
- Component design/selection
- Status
- Open, Classified
- Product code
- BRY
- Quantity affected
- 1 unit
- Distribution
- US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
- Date initiated
- 2026-04-30
- Date posted
- 2026-06-03
- Location
- San Diego, CA
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