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BD Pyxis MedStation 4000 Fingerprint Scanner
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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.

Recalled
Listed
Updated
Recall No.
Z-2297-2026
Agency
FDA
Firm
CareFusion 303, Inc.
Recall ID
98895
Status
ONGOING

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.

ProductLot codeRecall #UDI-DI
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinetAll Serial Numbers/UDI:10885403517167Z-2303-202610885403517167
BD Pyxis Mini Main REF: 349 Medication cabinetAll Serial Numbers/UDI:10885403512582Z-2301-202610885403512582
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinetAll Serial Numbers/UDI:10885403477829Z-2300-202610885403477829
BD Pyxis MedStation ES REF: 323 Medication cabinetAll Serial Numbers/UDI:10885403512667Z-2298-202610885403512667
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinetAll Serial Numbers/UDI:10885403477836Z-2299-202610885403477836
BD Pyxis MedStation 4000 REF: 303 Medication cabinetAll Serial Numbers/UDI:10885403512629Z-2297-202610885403512629
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinetAll Serial Numbers/UDI:10885403517181Z-2304-202610885403517181
BD Pyxis MedStation ES Tower REF: 352 Medication cabinetAll Serial Numbers/UDI:10885403512674Z-2302-202610885403512674

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other recent recalls from CareFusion 303, Inc.

All recalls from CareFusion 303, Inc.

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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