CareFusion recalls BD PYXIS medication dispensing cabinets with software version 3.9.1.9 due to potential incorrect bin labeling for medications. Affected units may print wrong storage locations for 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 medication dispensing cabinets with software version 3.9.1.9 because they might print incorrect storage bins for medications. This could lead to medications being misplaced in the wrong location within automated dispensing cabinets.
The software issue causes restock labels for medications to print with the wrong storage bin. This could lead to medications being placed in the incorrect location within automated dispensing cabinets, potentially causing medication errors.
Healthcare facilities using BD PYXIS medication dispensing cabinets with software version 3.9.1.9 are most likely affected. Staff handling medications in these cabinets could be at risk if the incorrect bin labels cause medication errors.
Check for BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow units with software version 3.9.1.9. The serial numbers listed in the recall notice include specific numbers like 16139674, 16124908, and others.
Verify the software version on your BD PYXIS cabinet. If it shows 3.9.1.9, it is affected.
The affected software version is 3.9.1.9.
Check if your cabinet has software version 3.9.1.9. The serial numbers listed in the recall include specific numbers like 16139674, 16124908, and others.
The recall does not specify a remedy, so you should contact CareFusion for further instructions.
We’ve drafted a message you can send BD PYXIS to request your refund or repair — edit it as you like.
Subject: Recall Z-2487-2024 — BD PYXIS BD PYXIS Hello, I own a BD PYXIS that is covered by recall Z-2487-2024 from BD PYXIS. 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.
