Class II

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

Covidien LLC · April 23, 2026

Reason for Recall

Temperature probe devices lack FDA clearance.

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.

States Affected

NATIONWIDE

Quantity Affected

1775 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2272-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Covidien LLC Medical Device Recall: Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 | SafeCheck