Bruder Healthcare recalls MediBeads King Pad pads with item numbers 34120, 34120PM, 34125R due to potential mold/mildew growth from moisture exposure. Affected lots include UPC 041533341208 and lot numbers M053590, M053280.
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 MediBeads King Pad moist heat compress pads with specific item numbers because they may have been exposed to excessive moisture, which could lead to mold or mildew growth. This poses a health risk if the pads are used without proper drying.
The pads may have been exposed to excessive moisture during manufacturing, which can cause mold or mildew to grow. If the pads are used without proper drying, this could lead to health issues like skin irritation or infections.
Users of MediBeads King Pad pads with item numbers 34120, 34120PM, or 34125R are most at risk if the pads have been exposed to excessive moisture. People using these products for medical purposes should check for mold or mildew.
Check the item numbers on the pads: 34120, 34120PM, or 34125R. Also look for lot numbers M053590 or M053280 on the packaging or label.
Inspect the pads for visible mold or mildew growth, especially in damp areas.
The recall states that pads from certain lots may have been exposed to excessive moisture, which could lead to mold or mildew growth. If you find mold or mildew, stop using them immediately.
Check the item numbers on the pads: 34120, 34120PM, or 34125R. Also look for lot numbers M053590 or M053280 on the packaging or label.
If you see mold or mildew growth, stop using the pads immediately and dispose of them safely.
We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1367-2024 — Bruder Healthcare Bruder Healthcare Hello, I own a Bruder Healthcare that is covered by recall Z-1367-2024 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.
