Covidien Mon-a-Therm Temperature Probe Recall
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
Updated April 23, 2026
Covidien Mon-a-Therm temperature probe (9 Fr, REF 90050) was sold without FDA clearance. The company initiated a voluntary withdrawal because these devices lack the required regulatory authorization.
Is the Covidien LLC recalled? Yes. This product was recalled by FDA on April 23, 2026. Details below.
What is recalled
Covidien Mon-a-Therm general purpose temperature probe, size 9 Fr, REF 90050.
Am I affected
You're affected if you own a Covidien Mon-a-Therm temperature probe with the reference number 90050 and size designation 9 Fr.
What to do right now
Stop using this temperature probe immediately. Contact Covidien LLC or your healthcare provider to arrange a return or replacement with a cleared device.
The hazard
Temperature probe devices lack FDA clearance.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2273-2026
- Classification
- Class II
- Recalled
- April 23, 2026
Get free recall alerts
New Medical Devices recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.
More Medical Devices recalls
Boston Scientific Rapid Refill Injection System Recall
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
ChloraPrep FREPP Applicators Recall
ChloraPrep FREPP sterile skin antiseptic applicators were distributed without proper sterilization, posing a risk of infection. These applicators are used …
CareFusion 213, LLC
Orthofix MINIRAIL M101 Recall
Orthofix MINIRAIL external fixation devices were shipped with incorrect model labels. The M101 was labeled as M103, the M103 was labeled as M101, and the M122 …
Orthofix U.S. LLC