Medline recalls pediatric drapes that may allow non-sterile product use if the breather pouch seal is opened. Affected kits have lot number 23LBL738. Consumers should check their product and follow official instructions.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling pediatric drapes that could lead to using non-sterile products if the breather pouch seal is opened. This poses a risk for infections during medical procedures.
The breather pouch seal on these drapes may open unintentionally, allowing non-sterile materials to be used during medical procedures. This could lead to infections if the drapes are not properly sealed.
Healthcare workers and parents using pediatric drapes for medical procedures are most at risk. The recall affects kits sold with lot number 23LBL738.
Check for lot number 23LBL738 on the product packaging. The product is a pediatric drape kit with reference number DYNJ81297.
Inspect the breather pouch seal for any signs of being opened or unsealed.
Reach out to Medline for guidance on whether the product is affected and next steps.
The recall indicates a potential risk of using non-sterile products if the breather pouch seal is opened, which could lead to infections during medical procedures.
Check for lot number 23LBL738 on the product packaging. The product is a pediatric drape kit with reference number DYNJ81297.
If the breather pouch seal is open or unsealed, do not use the product and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0169-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0169-2025 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.
