FDAFDA · Food and drugs·Recall number Z-2272-2026
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Published June 10, 2026 · Recall initiated: April 23, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Temperature probe devices lack FDA clearance.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Covidien LLC
- Distributor
- 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.
- Lot
- UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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