CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 due to potential incorrect medication bin printing. Affected units may mislabel medications in automated dispensing cabinets.
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 recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 because it can print the wrong medication bin on restock labels. This could lead to incorrect medication storage in automated dispensing cabinets.
The software issue causes restock labels for medications to show the incorrect storage bin. This could lead to medications being placed in the wrong location within automated dispensing cabinets.
Healthcare facilities using BD PYXIS MEDBANK TWR software version 3.9.1.9 are most at risk. This affects automated dispensing cabinets in hospitals and clinics.
Check for BD PYXIS MEDBANK TWR model CR-8HH-1FH-2FM-P with software version 3.9.1.9. The product has a UDI: 10885403512568 and serial number 15684798.
Verify the software version on your BD PYXIS MEDBANK TWR system. The affected version is 3.9.1.9.
The recall addresses a potential printing error that could lead to incorrect medication storage, but it does not pose an immediate risk of injury or harm.
Check for BD PYXIS MEDBANK TWR model CR-8HH-1FH-2FM-P with software version 3.9.1.9. The product has a UDI: 10885403512568 and serial number 15684798.
The official recall does not specify a remedy, so you should check the software version and contact CareFusion for guidance.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2500-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2500-2024 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.
