CareFusion recalls BD PYXIS MEDBANK TWR MN software version 3.9.1.9 due to potential incorrect medication bin labels during restocking. Affected units have specific serial numbers and model 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 recalls BD PYXIS MEDBANK TWR MN units with software version 3.9.1.9 because printing restock labels may show the wrong medication bin. This could lead to medication errors if staff follow the incorrect labels.
The software issue causes restock labels for medications in automated dispensing cabinets to print the wrong bin location. This could lead to staff placing medications in the incorrect storage area, potentially causing medication errors.
Healthcare facilities using BD PYXIS MEDBANK TWR MN units with software version 3.9.1.9 are most at risk. Staff handling medication restocking may encounter incorrect bin labels.
Check for BD PYXIS MEDBANK TWR MN model with serial numbers starting with 15806714 through 16203044 and software version 3.9.1.9. The product code is CR-10HH-2FH-P, REF: 169-82.
Verify the software version on your BD PYXIS MEDBANK TWR MN unit; affected units have version 3.9.1.9.
The software issue can cause restock labels to print the incorrect medication bin, potentially leading to medication errors if staff follow the wrong labels.
Check for BD PYXIS MEDBANK TWR MN with serial numbers starting with 15806714 through 16203044 and software version 3.9.1.9.
The recall does not specify a remedy, so no action is required beyond checking the software version.
We’ve drafted a message you can send BD PYXIS MEDBANK to request your refund or repair — edit it as you like.
Subject: Recall Z-2488-2024 — BD PYXIS MEDBANK BD PYXIS MEDBANK Hello, I own a BD PYXIS MEDBANK that is covered by recall Z-2488-2024 from BD PYXIS MEDBANK. 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.
