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Recall Observatory FDA recall evidence

Device product

Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044

Z-2272-2026

April 23, 2026

Class II

Product summary

Firm
Covidien LLC
Event
Event 98859
Status
Ongoing
Classification
Class II
Quantity
1775 units
Official record key
device-enforcement:Z-2272-2026

Official wording

Reason: Temperature probe devices lack FDA clearance.

Code information: UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Temperature probe devices lack FDA clearance.