Bruder Healthcare recalls Thermalon Stye Compresses (Item 24352) due to potential mold/mildew growth from moisture exposure in certain lots. Affected units sold with Lot M058520.
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 Stye Compresses (Item : 24352) because some units may have been exposed to excessive 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 too much moisture during manufacturing, creating conditions where mold or mildew can grow. If mold grows, it could cause eye irritation or infection when used.
Users of Thermalon Stye Compresses with Lot Number M058520 are affected. People using these compresses for eye infections are most at risk if mold grows.
Check for the lot number M058520 on the Thermalon Stye Compress packaging. The product has UPC 041533243526 and item number 24352.
Inspect the compress for visible mold or mildew before use.
If mold is found, discard the compress immediately and do not use it.
Yes, if no mold or mildew is visible, the compress can be used as long as it is dried properly.
Check the lot number on the packaging; if it's M058520, discard it if mold is present or contact Bruder Healthcare for guidance.
The recalled product has UPC 041533243526 and lot number M058520. Check the packaging for these identifiers.
We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1365-2024 — Bruder Healthcare Bruder Healthcare Hello, I own a Bruder Healthcare that is covered by recall Z-1365-2024 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.
