Thermalon Neck Wrap, Item Number 24322
FDA Recall #Z-1363-2024 — Class II — February 21, 2024
Product Description
Thermalon Neck Wrap, Item Number 24322
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.
Recalling Firm
Bruder Healthcare Company, LLC — Alpharetta, GA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
471 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Code Information
UPC 041533243229, Lot Numbers: M053560, M053140
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated