CareFusion recalls BD PYXIS MEDBANK TWR MN and MINI models due to a labeling update needed for procedure and operating room use. No immediate action required.
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
CareFusion is recalling several BD PYXIS MEDBANK TWR MN and MINI models because their labeling needs to include a contraindication statement against using medicine cabinets in procedures and operating rooms. This recall does not involve a safety hazard but requires updated labeling information.
The product labeling needs to include a contraindication statement to prevent the use of medicine cabinets during procedures and in operating rooms. This is a labeling update to ensure proper usage instructions, not a physical safety hazard.
Healthcare professionals using BD PYXIS MEDBANK TWR MN and MINI models in procedures or operating rooms. The risk is minimal as this is a labeling update rather than a safety issue.
Check for BD PYXIS MEDBANK TWR MN or MINI models with model numbers listed in the recall (e.g., 169-151, 169-152, 169-101, etc.). These products were sold with specific model numbers and serial codes.
Check if your product has a labeling update for procedure and operating room use as required by the recall.
No, this recall is for a labeling update to include a contraindication statement against using medicine cabinets in procedures and operating rooms. It does not pose a safety hazard.
No, the recall does not require stopping use. This is a labeling update to ensure proper usage instructions.
Check the model numbers listed in the recall, such as 169-151, 169-152, 169-101, etc., to determine if your BD PYXIS MEDBANK TWR MN or MINI model is affected.
We’ve drafted a message you can send Trsmima to request your refund or repair — edit it as you like.
Subject: Recall Z-1230-2025 — Trsmima Trsmima Hello, I own a Trsmima that is covered by recall Z-1230-2025 from Trsmima. 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.
