CareFusion recalls BD PYXIS MEDBANK TWR units with software version 3.9.1.9 for potential incorrect medication bin labeling during restock. Affected units have specific serial numbers and UDI.
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.
CareFusion is recalling BD PYXIS MEDBANK TWR units with software version 3.9.1.9 because printing restock labels may show the wrong medication bin. This could lead to incorrect medication dispensing if not fixed.
The software issue causes restock labels for medications in automated dispensing cabinets to print the wrong bin location. This might lead to medications being dispensed to the incorrect storage area, potentially causing errors in medication handling.
Healthcare facilities using BD PYXIS MEDBANK TWR units with software version 3.9.1.9 are most at risk. Patients and staff could be affected if incorrect medication bins are used.
Check for BD PYXIS MEDBANK TWR units with serial numbers 16210460, 16191229, 16227391, 16260053, or 16055232, 16102551. The software version 3.9.1.9 is also part of the affected units.
Verify the software version on your BD PYXIS MEDBANK TWR unit; if it is 3.9.1.9, it is affected.
The recall is for a potential labeling error that could lead to incorrect medication bins. It is not immediately dangerous but requires attention to prevent medication errors.
Check for serial numbers 16210460, 16191229, 16227391, 16260053, or 16055232, 16102551, or software version 3.9.1.9.
The recall does not specify a remedy, so contact CareFusion for guidance on next steps.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2489-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2489-2024 from CareFusion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
