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

FDA device recall Z-2272-2026 · posted 2026-05-29 · Open, Classified

Recall details

Recalling firm

Covidien LLC

Reason for recall

Temperature probe devices lack FDA clearance.

Action taken

On April 23, 2026 Covidien (subsidiary of Medtronic) issued a Urgent Medical Device Recall Notification to affected consignees via USPS. Covidien ask consignees to take the following actions: 1. Quarantine all unused product from the affected lots. 2. Return all unused product(s) from the affected lots in your inventory to Medtronic as described in the Customer Confirmation Form. 3. Share this notice with all relevant personnel within your organization, and with any organization to which the potentially affected product from the specified lots has been transferred or distributed. 4. Please complete and return the enclosed Customer Confirmation Form to rs.gmbmitgfca@medtronic.com even if you do not have unused inventory.

Root cause

Under Investigation by firm

Status

Open, Classified

Product code

BZT

Quantity affected

1775 units

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.

Date initiated

2026-04-23

Date posted

2026-05-29

Location

Boulder, CO