← FDA ENFORCEMENT
Z-2272-2026Class II
Covidien LLC
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Covidien LLC
Product type
Device
Status
Ongoing
Report date
2026-06-10
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.
Firm state
CO
Product quantity
1775 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Temperature probe devices lack FDA clearance.
Product description
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Code / lot info
UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →