CareFusion recalls BD Pyxis QFill Replenishment Station (REF: 138904-01) due to potential incorrect medication labels printed for non-CUBIE locations. 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 a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
CareFusion is recalling BD Pyxis QFill Replenishment Stations that may print incorrect medication labels when restocking from non-CUBIE locations. This could lead to the wrong medication being dispensed if users follow the labels.
The software issue causes restock labels for medications stored outside the CUBIE location to print the wrong medication bin. This could result in incorrect medications being dispensed if users follow the labels.
Healthcare facilities using the BD Pyxis QFill Replenishment Station with serial numbers 44210411, 43880801, or 44227426 are affected. Staff handling medication dispensing are most at risk.
Check for serial numbers 44210411, 43880801, or 44227426 on the BD Pyxis QFill Replenishment Station. The product is a medication cabinet system sold under the CareFusion brand.
Verify your unit has serial numbers 44210411, 43880801, or 44227426.
Due to a software issue that may print incorrect medication bins on restock labels for medications stored outside the CUBIE location.
Check if your unit has serial numbers 44210411, 43880801, or 44227426. If so, stop using it until you can confirm the labels are correct.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2947-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2947-2024 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.
