Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor… — Class II medical device recall Z-2271-2026
Ongoing recall by Covidien LLC, reported 2026-06-10, distributed nationwide. Temperature probe devices lack FDA clearance.
| Recall number | Z-2271-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, Boulder, CO, United States |
| Recall initiated | 2026-04-23 |
| Classified | 2026-05-29 |
| Reported by FDA | 2026-06-10 |
| Distributed | Nationwide (US) |
| Quantity | 23,000 units |
| UPC / GTIN / UDI-DI | 30884521820900 |
| Lot numbers | 25D1267JZX, 25E1322JZX, 25E1324JZX, 25H0920JZX |
| Model numbers | 90042 |
Product
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
Reason for recall
Temperature probe devices lack FDA clearance.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2271-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.