CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
- Recalling company
- CareFusion 303, Inc.
- Product
- BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
- Reason
- Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 30, 2026
- Reported
- Jun 10, 2026
- Distribution
- US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
- Status
- Ongoing
- Quantity
- 607 units
- Lot / codes
- All Serial Numbers/UDI:10885403517167
- Company location
- San Diego, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2303-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2303-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.