Reported Aug 14, 2024 · Ongoing
BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 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-4HH-P
- REF169-115 containing software version 3.9.1.9
- Lot codes and dates
- UDI10885403512544/
- Serial Number
232 of 232 codes
161706611621090816089019160624331614716916080412161249061594037515940373159403741594037615957620159576211594130715967410159674121596740915967413159674111596736115943774160569241618892815943781159434701594378215872417159024171590241815888968152537361525373716247094162839791622506916222611161655331620572716270832162004741624481016250223159356171565470715654706154892451572380315927979159245321556960815832680158326791582420615815815158158251541513615415135154151371541513815622987
- Amount recalled
- 232 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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