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MEDICAL DEVICE RECALLMODERATE
BD Pyxis MedStation 4000 Fingerprint Scanner
BD Pyxis MedStation 4000 recalled: fingerprint scanner may overheat, causing burns.
What to do
Stop using the fingerprint scanner on the affected BD Pyxis MedStation 4000 cabinet and contact BD for instructions on repair or replacement.
Why it was recalled
BD is recalling the Pyxis MedStation 4000 medication cabinet because the fingerprint scanner may overheat and cause first-degree burns. The affected product is the BD Pyxis MedStation 4000 with REF 303.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
| Product | Lot code | Recall # | UDI-DI |
|---|---|---|---|
| BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet | All Serial Numbers/UDI:10885403517167 | Z-2303-2026 | 10885403517167 |
| BD Pyxis Mini Main REF: 349 Medication cabinet | All Serial Numbers/UDI:10885403512582 | Z-2301-2026 | 10885403512582 |
| BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet | All Serial Numbers/UDI:10885403477829 | Z-2300-2026 | 10885403477829 |
| BD Pyxis MedStation ES REF: 323 Medication cabinet | All Serial Numbers/UDI:10885403512667 | Z-2298-2026 | 10885403512667 |
| BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet | All Serial Numbers/UDI:10885403477836 | Z-2299-2026 | 10885403477836 |
| BD Pyxis MedStation 4000 REF: 303 Medication cabinet | All Serial Numbers/UDI:10885403512629 | Z-2297-2026 | 10885403512629 |
| BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet | All Serial Numbers/UDI:10885403517181 | Z-2304-2026 | 10885403517181 |
| BD Pyxis MedStation ES Tower REF: 352 Medication cabinet | All Serial Numbers/UDI:10885403512674 | Z-2302-2026 | 10885403512674 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other recent recalls from CareFusion 303, Inc.
Editorial summary by Recall Canary · summary updated 2026-09-08 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification
