Covidien Llc: Stethoscope, Esophageal, With Electrical Conductors
Recall Summary Covidien LLC is recalling Mon-a-Therm esophageal temperature probes (model 90050, 9 Fr size) distributed nationwide because these devices lack required FDA clearance. The temperature probes were sold without the necessary regulatory approval for medical use. This Class II recall affects the product across all U.S. states and territories.
- Recalling firm
- Covidien LLC
- Product
- Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
- Reason
- Temperature probe devices lack FDA clearance.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-23
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/83af3873-24a7-4058-9e1f-716240996898