CareFusion recalls specific BD PYXIS MEDBANK models due to software error during pocket exchange restocking that could double medication counts and delay access to medicines.
Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
CareFusion is recalling specific BD PYXIS MEDBANK medication cabinets because a software error during restocking can cause medication counts to double, potentially delaying access to needed medicines. This could temporarily impair a person's ability to get medications they require.
When users try to restock a single bin location during pocket exchange restocking, the software may incorrectly process two stock transactions and two destock transactions. This doubles the medication count in that bin, which can delay access to medications and temporarily impair body function.
Healthcare facilities using the recalled BD PYXIS MEDBANK medication cabinets are most at risk. Patients relying on these cabinets for medication access could experience temporary delays in getting needed medicines.
Check if your BD PYXIS MEDBANK cabinet has the model numbers listed in the recall: MEDPASS MODULE (139088-01), MINI 1FH-1FM (169-137), MINI 1HH-1FH-1HM (169-101), or other specific models listed in the recall notice.
Look for the model number on your cabinet to see if it matches the recalled models listed in the notice.
The recall is due to a software issue that can cause medication counts to double during restocking, potentially delaying access to medicines.
The recall notice states this could lead to temporary body function impairment, but not serious injury or death.
Check if your cabinet has the specific model numbers listed in the recall notice, such as MEDPASS MODULE (139088-01) or MINI 1FH-1FM (169-137).
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-1639-2025 — BD PYXIS MEDBANK BD PYXIS MEDBANK Hello, I own a BD PYXIS MEDBANK that is covered by recall Z-1639-2025 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.
