CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 due to potential incorrect medication bin labeling 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 cabinets 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 cabinet is used.
The software issue causes restock labels for medications in automated dispensing cabinets to print the incorrect storage bin. This could lead to medications being placed in the wrong location, potentially causing medication errors.
Healthcare facilities using BD PYXIS MEDBANK TWR cabinets with software version 3.9.1.9 are most at risk. Patients receiving medication from these cabinets could be affected if labeling errors occur.
Check for BD PYXIS MEDBANK TWR cabinets with software version 3.9.1.9. The product has a serial number 15910847 and UDI 10885403512568.
Verify the software version on your BD PYXIS MEDBANK TWR cabinet. The affected version is 3.9.1.9.
The recall addresses a potential labeling error that could lead to medication errors, but it does not indicate immediate risk of serious injury.
Check for BD PYXIS MEDBANK TWR cabinets with software version 3.9.1.9, which has a serial number 15910847 and UDI 10885403512568.
The official 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-2493-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2493-2024 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.
