PlainRecalls
FDA Devices Moderate Class II Ongoing

Thermalon Back Wrap, Item Number 24312

Reported: April 3, 2024 Initiated: February 21, 2024 #Z-1362-2024

Product Description

Thermalon Back Wrap, Item Number 24312

Reason for Recall

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Details

Units Affected
193 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Location
Alpharetta, GA

Frequently Asked Questions

What product was recalled?
Thermalon Back Wrap, Item Number 24312. Recalled by Bruder Healthcare Company, LLC. Units affected: 193 units.
Why was this product recalled?
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 3, 2024. Severity: Moderate. Recall number: Z-1362-2024.