Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 recall (Covidien LLC)
Medical deviceClass IIOngoing
Summary: Covidien LLC is recalling Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044. Reason: Temperature probe devices lack FDA clearance.
What is being recalled
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Why
Temperature probe devices lack FDA clearance.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV. (states named: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Hawaii, Illinois, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Tennessee, Texas, Utah, Virginia, Washington, West Virginia)
How to tell if yours is affected
UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2272-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | April 23, 2026 |
| Reported | June 10, 2026 |
| Company | Covidien LLC |
| Company location | Boulder, CO, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1775 units |
More recalls from Covidien LLC · all medical device recalls · recalls from April 2026