Medline recalls leg bags with specific lot numbers due to undeclared latex. Consumers should check their product details to determine if affected.
Undeclared latex
Medline is recalling leg bags with the model reference DYND12574 because they contain undeclared latex. This could cause allergic reactions in sensitive individuals.
The leg bags contain undeclared latex, which can cause allergic reactions in people sensitive to latex. This is a potential health risk for individuals with latex allergies.
People who own or use Medline leg bags with the model reference DYND12574 and specific lot numbers are affected. Those with latex allergies are at higher risk.
Check for the model reference DYND12574 on the bag. Look for lot numbers 48623040001, 48623050001, 48623060001, or 48623080001.
Identify the model reference (DYND12574) and lot numbers (48623040001, 48623050001, 48623060001, 48623080001) to confirm if your bag is affected.
The recall does not require stopping use immediately; check if your bag has the specific model and lot numbers to determine if it's affected.
The recall record does not specify a remedy, so contact Medline directly for further instructions.
Check for the model reference DYND12574 and lot numbers 48623040001, 48623050001, 48623060001, or 48623080001.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0533-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-0533-2024 from Medline. 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.
