Reported Dec 18, 2024 · Ongoing
BD Pyxis MedStation ES, REF: 323
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
- REF323
- Lot codes and dates
- All software versions
- REF/UDI-DI1
3,607 of 3,607 codes
323/10885403512667/1244110312440974124409751244133312441432124476841245549312455498124554921245579312458864124636121247084212476547124825321248339312486737124990431249983812499616124996171249961812505982125083031251421612514218125142171251422012515358125229421252793012528710125287091253009012531418125373641253736312537076125401961254019412540267125402681254026912561139125686971256917012570749125707501257074512570746125707481257075312585184125851831258628512589659125896851258965812589618
- Amount recalled
- 98,526
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
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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