Bruder Healthcare recalls Thermalon Neck Wraps (Item 24322) with specific lot numbers due to potential mold/mildew growth from 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 Thermalon Neck Wraps from certain lots 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 wraps are used without proper cleaning.
The neck wraps may have been exposed to excessive moisture during manufacturing, which can allow mold and mildew to grow. If the wraps are used without proper cleaning, mold spores could be inhaled or come into contact with skin, causing health issues.
People who own or use Thermalon Neck Wraps with lot numbers M053560 or M053140 are affected. Those using the wraps for medical purposes are at slightly higher risk due to potential health impacts from mold.
Check the lot number on the Thermalon Neck Wrap packaging. Affected units have lot numbers M05356: M053560 or M053140. The product is sold under UPC 041533243229.
Look for lot numbers M053560 or M053140 on the Thermalon Neck Wrap packaging.
The Thermalon Neck Wraps from certain lots may have been exposed to excessive moisture, which can lead to mold and mildew growth.
The recall record does not specify a remedy, so check the lot number and contact Bruder Healthcare for further instructions.
The recall states potential mold/mildew growth from moisture exposure, but no specific serious injury risk is mentioned.
We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1363-2024 — Bruder Healthcare Bruder Healthcare Hello, I own a Bruder Healthcare that is covered by recall Z-1363-2024 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.
