Reported Aug 14, 2024 · Ongoing
BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9
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 MDBNK TWR MN CR-4HH-5FM-P RxNow
- REF169-131 containing software version 3.9.1.9
- Lot codes and dates
- UDI10885403512568/
- Serial Number
61 of 61 codes
161396741612490816063924160844671622154916139675162208751623725816284001159404001594010415941703159416541594375015943749155006961565471115654721156310991563110415775749153834801538348115383475153834861538348715366328156061701557597415575976154907451542213315853047159024131559809515550853154378091543781215518269155182731551827015872432158724291566281615504833155048361550351115430948154309631563968715639724156397201563971815328493154427941544278915761398157614011593757915786154
- Amount recalled
- 61 units
This recall covers 19 products
The agency filed one notice per product. You are reading one of them; the other 18 are below.
6 more are in the archive.
Where it was sold
Why it was recalled
Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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