- Recalling firm
- Covidien LLC
- Reason for recall
- Temperature probe devices lack FDA clearance.
- Affected products (lot / model / serial)
- UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX
- Units affected
- 1775 units
- 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.
- Firm location
- Boulder, CO, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2272-2026
- Recall initiated
- April 23, 2026
- FDA classification date
- May 29, 2026
- FDA report date
- June 10, 2026
- FDA event ID
- 98859
- Last updated on HTM Vibe
- July 23, 2026