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Covidien Mon-a-Therm Esophageal Stethoscope
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MEDICAL DEVICE RECALLMODERATE

Covidien Mon-a-Therm Esophageal Stethoscope

Covidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.

What to do

Stop using the recalled device immediately. Contact Covidien for instructions on returning the device and for information on replacement or remediation.

Recalled
Listed
Updated
Recall No.
Z-2271-2026
Agency
FDA
Firm
Covidien LLC
Recall ID
98859
Status
ONGOING

Why it was recalled

Covidien is recalling the Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM (REF 90042) because the temperature probe devices lack FDA clearance. The affected device is used to monitor patient temperature during surgery.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

ProductLot codeRecall #UDI-DI
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 9005024D1130JZX, 25A1086JZX, 25E1332JZX, 25I1054JZX, 24D1133JZX, 25A1087JZX, 25F0946JZX, 25I1055JZX, 24E1015JZX, 25A1088JZX, 25F0947JZX, 25I1056JZX, 24E1017JZX, 25D0379JZX, 25F0948JZX, 25I1057JZX, 24E1018JZX, 25D0380JZX, 25F0949JZX, 25I1058JZX, 24L0848JZX, 25D0381JZX, 25F0950JZX, 25I1059JZX, 24L0850JZX, 25D1271JZX, 25F0953JZX, 25I1061JZX, 25A1069JZX, 25D1272JZX, 25F0954JZX, 25K1129JZX, 25A1070JZX, 25D1273JZX, 25G1163JZX, 25K1130JZX, 25A1072JZX, 25E1263JZX, 25H0935JZX, 25K1131JZX (+21 more, see the official notice)Z-2273-202610884521828391, 30884521828395
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 9004425F0945JZX, 25H0949JZX, 25I1065JZX, 25I1066JZXZ-2272-202630884521828388
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 9004225D1267JZX, 25E1322JZX, 25E1324JZX, 25H0920JZXZ-2271-202630884521820900

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification