FDA DevicesClass II
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Published: June 10, 2026Recall ID: Z-2272-2026Category: devicesCountry: US
Reason for Recall / Hazard
Temperature probe devices lack FDA clearance.
Product Description & Identification
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Affected Products
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Additional Source Details
| Field | Value |
|---|---|
| City | Boulder |
| State | CO |
| Event id | 98859 |
| Address 1 | 6135 Gunbarrel Ave |
| Code info | UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX |
| Postal code | 80301-3214 |
| Report date | 20260610 |
| Product type | Devices |
| Product quantity | 1775 units |
| Reason for recall | Temperature probe devices lack FDA clearance. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260423 |
| Initial firm notification | |
| Center classification date | 20260529 |
Overview
- Recalling FirmCovidien LLC
- StatusOngoing
- Risk LevelClass II
- DistributionUS 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.