CareFusion recalls BD PYXIS MEDBANK MINI models with labeling update to include contraindication against use in procedures and operating rooms.
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
CareFusion is recalling specific BD PYXIS MEDBANK MINI models due to a labeling update that adds a contraindication statement against using these devices in procedures and operating rooms. This change is to address potential risks when these devices are used in medical settings.
The hazard involves a labeling update that adds a contraindication statement. This means the device should not be used in procedures or operating rooms. The risk is low as it's a labeling change to ensure safe usage in specific medical settings.
Patients and healthcare providers who use the BD PYXIS MEDBANK MINI devices in procedures or operating rooms may be affected. The risk is low as this is a labeling update to clarify contraindications.
Check for BD PYXIS MEDBANK MINI models with serial numbers listed in the recall (e.g., 138913-01, 138911-01, 138912-01, etc.) sold between 2010 and 2023.
Verify if your device has the specific model numbers listed in the recall notice.
The recall is for a labeling update to include a contraindication statement against using the device in procedures and operating rooms.
No, this is a labeling update to clarify contraindications. The device can still be used in non-procedure settings.
Check if your device has the specific model numbers listed in the recall notice. No action is needed if it's not listed.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1227-2025 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1227-2025 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.
