Recall of BD Pyxis MEDBANK Mini CR-4HH-P units with software version 3.9.1.9 due to potential printing of incorrect medication bins. Affected units have specific serial numbers.
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 Mini units with software version 3.9.1.9 because they may print incorrect medication bins when restocking. This could lead to wrong medication being dispensed if not corrected.
The software issue causes restock labels for medications in automated dispensing cabinets to print the wrong storage bin. This might result in the wrong medication being dispensed if staff follow the incorrect label.
Healthcare facilities using BD Pyxis MEDBANK Mini units with software version 3.9.1.9 are most at risk. Patients and staff could receive incorrect medications if the labeling error occurs.
Check if your unit has the model name 'BD PYXIS MEDBANK MINI CR-4HH-P' and software version 3.9.1.9. Serial numbers listed in the recall include many 15-digit numbers starting with 159 or 160.
Verify your unit's software version by checking the device settings or documentation.
Software version 3.9.1.9.
Check for the model 'BD PYXIS MEDBANK MINI CR-4HH-P' and software version 3.9.1.9. Affected units have specific serial numbers listed in the recall.
The recall does not specify a fix or remedy.
We’ve drafted a message you can send BD Pyxis to request your refund or repair — edit it as you like.
Subject: Recall Z-2486-2024 — BD Pyxis BD Pyxis Hello, I own a BD Pyxis that is covered by recall Z-2486-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
