Reported Aug 14, 2024 · Ongoing
BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 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 MEDBANK MINI CR-2HH-1FH-P
- REF169-114 containing software version 3.9.1.9
- Lot codes and dates
- UDI10885403512544/
- Serial Number
84 of 84 codes
161326581616837416097985161912271622155716203700161982961603479316207656162215561622506716138830160397641595039516042993159673601537811816155519160902031621608316112389160359481625635715940923159401501596196815950397159503991605523315442769162435531583265316085678160440381604404216044015160440161604401916044022160440211604403416044026160440321604402716044029160440311604404615499064159488541549076715631138153781201537812115409640159108421535391915547821150495111561800615371604
- Amount recalled
- 84 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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