Covidien recalls Mon-a-Therm temperature probes (size 9 Fr REF 90050) due to lack of FDA clearance. Affected units have specific UDI and lot numbers. Consumers should contact the manufacturer for details.
Temperature probe devices lack FDA clearance.
Covidien is recalling Mon-a-Therm temperature probes that lack FDA clearance. This means the devices may not be safe for medical use, potentially causing harm if used improperly.
The probes lack FDA clearance, meaning they have not been approved for medical use by the U.S. Food and Drug Administration. This could lead to inaccurate temperature readings or other safety issues during medical procedures.
Healthcare professionals using these probes for temperature monitoring are most at risk. Patients receiving care with these devices could be exposed to potential safety issues.
Check for the model number 'Mon-a-Therm size 9 Fr REF 90050' on the device. Look for the unique device identifier (UDI) numbers listed in the recall notice, such as 10884521828391 or 30884521828395.
Review the unique device identifier (UDI) and lot numbers listed in the recall notice to confirm if your device is affected.
The temperature probes lack FDA clearance, meaning they have not been approved for medical use by the U.S. Food and Drug Administration.
Check for the model number 'Mon-a-Therm size 9 Fr REF 90050' and the unique device identifier (UDI) numbers listed in the recall notice, such as 10884521828391 or 30884521828395.
The recall notice does not specify a remedy, so contact Covidien LLC directly for further instructions.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2273-2026 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2273-2026 from Covidien. 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.
