Thermalon Neck Wrap recalled over fire hazard
- Recall date
- February 21, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Bruder Healthcare Company, LLC recalls Thermalon Neck Wrap, Item Number 24322
- Recall number
- Z-1363-2024
- FDA classification
- Class II
- Brand / firm
- Bruder Healthcare Company, LLC
- Sold / distributed
- Worldwide distribution - US Nationwide and the country of Canada.
Why it was 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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Thermalon Neck Wrap, Item Number 24322
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