Bruder Healthcare recalls Thermalon Eye Compress (Item 2434) due to potential mold/mildew growth from moisture exposure. Affected lots may need disposal.
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 Eye Compress (Item : 2434) because certain lots may have been exposed to excessive moisture, which could lead to mold or mildew growth. This poses a health risk if the compress is used after mold develops.
Excessive moisture in certain lots can cause mold or mildew to grow inside the compress. Using moldy compresses could lead to skin irritation or infections, especially for people with sensitive skin or weakened immune systems.
People who own or use Thermalon Eye Compress (Item 2434) from specific lots are affected. Those with compromised immune systems or sensitive skin may be at higher risk.
Check for the item number 2434 on the packaging. Affected lots have specific lot codes: M056410. The UPC code is 041533243427.
Look for the lot code M056410 on the packaging to identify affected units.
The recall states that certain lots may have been exposed to excessive moisture, which could lead to mold or mildew growth. If mold is present, it may cause skin irritation or infection.
Check the lot code on the packaging. Affected units have the lot code M056410 and item number 2434 with UPC 041533243427.
The recall does not specify a remedy, so you should check with Bruder Healthcare for guidance on safe disposal or alternatives.
We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1359-2024 — Bruder Healthcare Bruder Healthcare Hello, I own a Bruder Healthcare that is covered by recall Z-1359-2024 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.
