CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 due to potential incorrect medication bin labeling in automated dispensing cabinets. Affected units have specific serial numbers and UDI codes.
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 they may print the wrong medication storage bin on labels. This could lead to medication errors if the wrong bin is used.
The software issue causes restock labels for medications in automated dispensing cabinets to print the incorrect storage bin. This could result in medications being placed in the wrong location, potentially causing medication errors.
Healthcare facilities using BD PYXIS MEDBANK TWR systems with the specific software version and serial numbers listed. Staff handling medication dispensing are most at risk of potential errors.
Check for the model number BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P with software version 3.9.1.9. Affected units have serial numbers 16042128, 16042129, 16044049, or 16044052 and UDI code 10885403512568.
Verify the software version on your BD PYXIS MEDBANK TWR unit to see if it is 3.9.1.9.
Reach out to CareFusion for guidance on next steps if you have the affected software version.
Software version 3.9.1.9.
Serial numbers 16042128, 16042129, 16044049, and 16044052.
Check for the model number BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P with software version 3.9.1.9 and the listed serial numbers or UDI code.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2495-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2495-2024 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.
