Medium risk Medical DevicesClass II

Covidien Mon-a-Therm Temperature Probe Recall

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Updated April 23, 2026

Covidien Mon-a-Therm temperature probe (9 Fr, REF 90050) was sold without FDA clearance. The company initiated a voluntary withdrawal because these devices lack the required regulatory authorization.

Is the Covidien LLC recalled? Yes. This product was recalled by FDA on April 23, 2026. Details below.

What is recalled

Covidien Mon-a-Therm general purpose temperature probe, size 9 Fr, REF 90050.

Am I affected

You're affected if you own a Covidien Mon-a-Therm temperature probe with the reference number 90050 and size designation 9 Fr.

What to do right now

Stop using this temperature probe immediately. Contact Covidien LLC or your healthcare provider to arrange a return or replacement with a cleared device.

The hazard

Temperature probe devices lack FDA clearance.

Brands affected

Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2273-2026
Classification
Class II
Recalled
April 23, 2026
Read the official notice

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