Reported Jan 29, 2025 · Ongoing
BD Pyxis MedStation ES AUX, REF 324
CareFusion 303, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- BD Pyxis MedStation ES AUX, REF 324
- Lot codes and dates
- UDI/DI 10885403512681
- Serial Numbers
3,260 of 3,260 codes
9418071941811094181249525533952553495255599525563952558395256019525603952560495256079525614952561595256169525617952561895256299526868952885695288579528924952893195291449529535953092495312519531255953125896324329632438963245212440840124408411244820712448208124522521245226412455476124576001245760112462734124627351246367612468607124686081246860912468610124686111246861212468670124686711246867212468673124686741247380712473808124738091247381012473811
- Amount recalled
- 39615 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Why it was recalled
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,
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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