FDAFDA · Food and drugs·Recall number Z-2300-2026
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Published June 10, 2026 · Recall initiated: April 30, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion 303, Inc.
- Distributor
- US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
- Lot
- All Serial Numbers/UDI:10885403477829
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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