Class II

Medical Device Recall: Thermalon Back Wrap, Item Number 24312

Bruder Healthcare Company, LLC · February 21, 2024

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.

Distribution

Worldwide distribution - US Nationwide and the country of Canada.

States Affected

NATIONWIDE

Quantity Affected

193 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1362-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.