CareFusion 303 BD Pyxis Medication Cabinets
BD Pyxis medication cabinets have a fingerprint scanner that may overheat and cause first-degree burns.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
CareFusion 303, Inc. of San Diego, California, began a recall of BD Pyxis medication cabinets on April 30, 2026, because the fingerprint scanner may overheat to a temperature to cause 1st degree burn.
The affected products include BD Pyxis MedBank Tower, BD Pyxis Mini Main, BD Pyxis Anesthesia Station 4000, BD Pyxis MedStation ES, BD Pyxis Anesthesia Station ES, BD Pyxis MedStation 4000, BD Pyxis MedBank Mini, and BD Pyxis MedStation ES Tower.
The recall was added to the FDA's Enforcement Report on June 3, 2026, and distributed nationwide in the U.S. and to AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
8 products
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
- UDI-DI
- 10885403512629
- Lot
- All Serial Numbers/UDI:10885403512629
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
- UDI-DI
- 10885403517167
- Lot
- All Serial Numbers/UDI:10885403517167
BD Pyxis Mini Main REF: 349 Medication cabinet
- UDI-DI
- 10885403512582
- Lot
- All Serial Numbers/UDI:10885403512582
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
- UDI-DI
- 10885403477829
- Lot
- All Serial Numbers/UDI:10885403477829
BD Pyxis MedStation ES REF: 323 Medication cabinet
- UDI-DI
- 10885403512667
- Lot
- All Serial Numbers/UDI:10885403512667
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
- UDI-DI
- 10885403477836
- Lot
- All Serial Numbers/UDI:10885403477836
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
- UDI-DI
- 10885403517181
- Lot
- All Serial Numbers/UDI:10885403517181
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
- UDI-DI
- 10885403512674
- Lot
- All Serial Numbers/UDI:10885403512674
Details
- Company began the recall
- Sold in
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
- Event ID
- 98895
- Recall numbers
- Z-2297-2026 to Z-2304-2026
- Company
- CareFusion 303, Inc.San Diego, California
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
