Class II

Medical Device Recall: Thermalon Sinus Compress (French), Item Number 24332F

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

2160 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1360-2024

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.

Bruder Healthcare Company, LLC Medical Device Recall: Thermalon Sinus Compress (French), Item Number 24332F | SafeCheck