Recall of BD Pyxis MedBank Mini and TWR MN units for labeling update to include contraindication against use in procedures and operating rooms. No action required for safety.
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
CareFusion recalls specific BD Pyxis MedBank Mini and TWR MN units to update labeling with a contraindication statement. This means these units should not be used in procedures or operating rooms. No action is needed for safety.
The recall involves updating labeling to include a contraindication statement. This means the units should not be used in procedures or operating rooms. The hazard is a labeling update to prevent misuse in high-risk environments.
Users of BD Pyxis MedBank Mini and TWR MN units in healthcare settings. The most at-risk are medical professionals using these units in procedures or operating rooms.
Check for BD Pyxis MedBank Mini units with model numbers like 1FH-1FM, 1HH-1HM, 2HH-1FH, etc., and TWR MN units with model numbers like 10HH-2FH, 12HH-1FF, etc. The units are sold with specific serial numbers and part numbers listed in the recall.
Review the product label for the specific model numbers listed in the recall to confirm if it is affected.
No action is required for safety. The recall is for labeling updates to prevent misuse in procedures and operating rooms.
The affected units include specific model numbers like 1FH-1FM, 1HH-1HM, 2HH-1FH, and TWR MN units with model numbers like 10HH-2FH, 12HH-1FF, etc., as listed in the recall.
The recall is for labeling updates to prevent misuse in procedures and operating rooms. No injury risk is associated with normal use.
We’ve drafted a message you can send BD Pyxis to request your refund or repair — edit it as you like.
Subject: Recall Z-1228-2025 — BD Pyxis BD Pyxis Hello, I own a BD Pyxis that is covered by recall Z-1228-2025 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.
