Medline recalls convenience kits that may allow non-sterile product use if breather pouch seal is opened. Affected kits have specific lot numbers and model references. Consumers should check their kits and contact Medline for details.
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 medical procedure convenience kits that could lead to using non-sterile products if the breather pouch seal is opened. This risk is serious because medical procedures require sterile conditions.
The breather pouch seal on these kits may open or become unsealed, allowing non-sterile products to be used during medical procedures. This can compromise infection control and patient safety.
Medical professionals and facilities using Medline convenience kits with specific lot numbers and model references are most at risk. Patients receiving procedures using these kits could be affected if non-sterile products are used.
Check for the model numbers: UNIVERSAL DRAPE PACK (REF DYNJ44114) or DRAPE PACK (REF DYNJ82663B). Lot numbers 24ABB398 or 23LBV498 indicate affected kits.
Inspect the breather pouch seal for signs of being opened or unsealed.
Reach out to Medline for specific guidance on affected kits and next steps.
The breather pouch seal on certain Medline convenience kits may open or become unsealed, allowing non-sterile products to be used during medical procedures.
Check for model numbers: UNIVERSAL DRAPE PACK (REF DYNJ44114) or DRAPE PACK (REF DYNJ82663B) with lot numbers 24ABB398 or 23LBV498.
Contact Medline for specific guidance on affected kits and next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0171-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0171-2025 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.
