Bruder Healthcare recalls French-language Thermalon Sinus Compresses with specific lot numbers due to potential mold/mildew growth from excessive moisture exposure. Affected units may need replacement.
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.
Bruder Healthcare is recalling certain French-language Thermalon Sinus Compresses because they might have been exposed to too much moisture, which could lead to mold or mildew growth. This poses a health risk if the compresses are used without proper drying.
The compresses may have been exposed to excessive moisture during manufacturing, which can allow mold and mild: mildew to grow. Using these compresses could lead to health issues if mold spores are inhaled or come into contact with skin.
People who own or use the recalled Thermalon Sinus Compresses (French version) with specific lot numbers are affected. Those with sensitive skin or allergies may be at higher risk from mold exposure.
Check the lot numbers on the product: M053600 or M053340. The product is sold under UPC 041533243328 and is labeled in French.
Look for lot numbers M053600 or M053340 on the Thermalon Sinus Compress packaging.
The recall is due to potential mold and mildew growth from excessive moisture exposure during manufacturing.
Check the lot number on your product. If it matches M053600 or M053340, stop using it and contact Bruder Healthcare for replacement.
The recall indicates potential mold/mildew growth, but no specific serious injury risk is mentioned in the official notice.
We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1360-2024 — Bruder Healthcare Bruder Healthcare Hello, I own a Bruder Healthcare that is covered by recall Z-1360-2024 from Bruder Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
