CareFusion recalls PYXIS MEDBANK MINI units with software version 3.9.1.9 due to potential printing of incorrect medication bins. Affected units have specific serial numbers and were sold with this software version.
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 is recalling PYXIS MEDBANK MINI units with software version 3.9.1.9 because they may print incorrect medication bins when restocking. This could lead to the wrong medication being dispensed, which is a serious safety risk for healthcare facilities.
The software issue causes restock labels for medications to print the wrong bin location. This means staff might dispense the incorrect medication from the wrong cabinet, potentially causing errors in patient treatment.
Healthcare facilities using the PYXIS MEDBANK MINI with software version 3.9.1.9 are most at risk. This includes hospitals and clinics that rely on automated medication dispensing systems.
Check if your PYXIS MEDBANK MINI has software version 3.9.1.9. The product includes specific serial numbers listed in the recall notice. Units sold with this software version are affected.
Verify your device's software version by checking the device settings or documentation.
Contact CareFusion to update to a corrected software version if your device is affected.
Software version 3.9.1.9 is affected.
Check if your PYXIS MEDBANK MINI has software version 3.9.1.9, as listed in the recall notice with specific serial numbers.
Contact CareFusion to update to a corrected software version to prevent incorrect medication labeling.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2485-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2485-2024 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.
