FDA Device recall Z-2272-2026
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- FDA Device
- Class II
- ongoing
- Published 2026-06-10
On 2026-06-10 the FDA classified a Class II recall of Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 by Covidien, citing temperature probe devices lack FDA clearance.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2272-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-23 |
| Published | 2026-06-10 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Covidien |
| Distribution | US |
Product
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Reason
Temperature probe devices lack FDA clearance.
Identifiers
| code_info | UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2272-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.