Covidien LLC recalls Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- Recalling company
- Covidien LLC
- Product
- Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- Reason
- Temperature probe devices lack FDA clearance.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 23, 2026
- Reported
- Jun 10, 2026
- Distribution
- 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.
- Status
- Ongoing
- Quantity
- 1775 units
- Lot / codes
- UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX
- Company location
- Boulder, CO
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2272-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2272-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.