Recall Weekly
Moderate riskFDA DeviceClass II

Physitemp MT-D temperature monitors recalled for unreviewed safety

Physitemp Instruments is recalling MT-D temperature monitors and their associated probes because they have not been reviewed for safety and effectiveness for their intended use. The recall covers lot codes distributed from January 19, 2024 through January 19, 2026, and 36 units are affected. No injuries have been reported.

From the FDA notice · Read the official notice ↗

What to do

  1. Stop using affected MT-D monitors and probes, and set them aside.
  2. Identify affected units by lot codes distributed between January 19, 2024 and January 19, 2026.
  3. The notice does not say how to get a replacement or refund; contact Physitemp Instruments.
Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Physitemp MT-D REF: MT-D
Sold in
Nationwide
Made for
All ages (0 months and older)

This recall covers 10 products — see all of them.

Details

Units affected
36 units
Illnesses reported
None reported
Manufactured in
189 Sargeant Ave, Clifton, New Jersey, United States
Classification
Class II
Recall number
Z-0404-2027

In the FDA's words

Description
Physitemp MT-D REF: MT-D Temperature monitors and associated probes have not been reviewed for safety and effectiveness for intended use. All lot codes distributed between January 19, 2024 through January 19, 2026. Distribution: Worldwide - US Nationwide distribution in the states of AR, MA, CA, PA, NY, IN, MD, KS, FL, LA, WA, WI, FL, CT, VA, OH, TX, MN, GA, UT and the countries of Japan, Canada, Australia, China, France, Sweden, England. Affected quantity: 36 units
Hazard
Temperature monitors and associated probes have not been reviewed for safety and effectiveness for intended use.

10 products in this recall

Physitemp temperature monitors and probes recalled, not safety reviewed

Physitemp Instruments is recalling 10 Physitemp temperature monitors and probes, including rectal, esophageal, skin, oral and general-purpose probes and Thermalert monitoring thermometers. The FDA says these devices have not been reviewed for safety and effectiveness for their intended use. The FDA classified the recall as Class II, and no injuries have been reported.

The agency lists each product separately. Check every one you might have.

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