Reported Jan 29, 2025 · Ongoing
BD Pyxis MedStation 4000 AUX, REF 306
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 4000 AUXREF 306
- Lot codes and dates
- UDI/DI 10885403512636
- Serial Numbers
3,261 of 3,261 codes
9304700930572393093029413001941301494156029415665941731194173129417335941734094174289417430941743394174379418065941806894181009418105941811194181129418113941811494181159418129941856895236799525535952555895255609525561952556295255829525590952560095256059525606952561395256249525630952563895256569525657952686795285309528836952885995288909531253953125712439518124395201243952112439907124402081244021712440218124402191244022012440227
- Amount recalled
- 5056 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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