← FDA ENFORCEMENT
Z-2272-2026Class II

Covidien LLC

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 openFDA enforcement API. 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.