CareFusion recalls BD Pyxis Mini Main REF 349 medication cabinets due to fingerprint scanner overheating that may cause first-degree burns. Affected units have specific serial numbers.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion is recalling BD Pyxis Mini Main REF 349 medication cabinets because the fingerprint scanner can overheat and cause first-degree burns. This risk affects healthcare workers who use the device daily.
The fingerprint scanner in the BD Pyxis Mini Main REF 34: 349 medication cabinet can overheat to a temperature that causes first-degree burns. This happens when the scanner is used repeatedly without proper cooling, leading to heat buildup.
Healthcare workers using the BD Pyxis Mini Main REF 349 medication cabinets are most at risk due to frequent contact with the fingerprint scanner. Patients and staff in medical facilities that use this device may also be affected.
Check for the BD Pyxis Mini Main REF 349 medication cabinet with serial numbers starting with 10885403512582. This model was sold with specific serial numbers listed in the recall notice.
Verify your device's serial number starts with 10885403512582 to confirm it is affected.
The recall states the fingerprint scanner may overheat and cause first-degree burns, so it is not safe to use without checking the serial number.
Affected devices have serial numbers starting with 10885403512582. Check your device's serial number to confirm.
The recall does not specify a remedy, so you should check the serial number to see if it is affected and contact CareFusion for further instructions.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2301-2026 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2301-2026 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.
