BD recalls Pyxis Med 4000 Auxiliary pumps with serial numbers 16140589-16079165 due to potential drawer or door failures that could delay medication access. Affected units may require repair or replacement.
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
BD is recalling Pyxis Med 4000 Auxiliary pumps that could have drawer or door failures, potentially delaying access to medications. This is a safety issue for healthcare facilities using these pumps.
Drawer and door failures in the Pyxis Med 4000 Auxiliary pumps could delay access to medications. This happens due to three issues: door latch failure, cable ribbon damage, or a magnet falling out.
Healthcare facilities using BD Pyxis Med 4000 Auxiliary pumps with specific serial numbers are most at risk. Patients receiving medications through these pumps may be affected if the device malfunctions.
Check for serial numbers 16140589, 16194078, 16194079, 16194081, or 16079165 on the device. The product is a BD Pyxis Med 4000 Auxiliary pump (REF 314).
Verify your device's serial number against the list: 16140589, 16194078, 16194079, 16194081, 16079165.
The recall is due to potential drawer and door failures that could delay access to medications, caused by door latch failure, cable ribbon damage, or a magnet falling out.
The official notice does not specify a remedy, so contact BD directly for guidance.
Check for serial numbers 16140589, 16194078, 16194079, 16194081, or 16079165 on the BD Pyxis Med 4000 Auxiliary pump (REF 314).
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-0976-2025 — BD BD Hello, I own a BD that is covered by recall Z-0976-2025 from BD. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
