Home › Covidien LP › Mon-a-Therm
Mon-a-Therm
Covidien LP · Model 90041 · UDI-DI 10884521820890
BZT
Prescription
2
510(k) clearances
30
Adverse events
4
Recalls
23
Facilities
Description
Esophageal Stethoscope with Temperature Sensor 400TM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-23 | Covidien LLC | Temperature probe devices lack FDA clearance. |
| 2026-04-23 | Covidien LLC | Temperature probe devices lack FDA clearance. |
| 2026-04-23 | Covidien LLC | Temperature probe devices lack FDA clearance. |
| 2011-09-26 | Cincinnati Sub-Zero Products Inc | Reports that the Rectal/ Esophageal Temperature Probes are not reading correctly. This situation causes the Blanketrol device, which the probes connect to, to shut down operation a |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.