Medline recalls 110+ medical procedure convenience kits with potential non-sterile product if breather pouch seals are opened. Affected kits include EYE PACK, PHACO PACK, and others with specific model numbers and lot numbers.
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 110 different medical procedure convenience kits that may contain non-sterile products if the breather pouch seal is opened. This risk could lead to infections or other complications during medical procedures.
The breather pouches in these kits have a vendor seal that can be opened or unsealed, potentially allowing non-sterile product to be used during medical procedures. This could lead to infections or other complications if the seal is compromised.
Healthcare professionals and medical facilities that use these kits for eye or cataract surgery. The risk is low for most users as the kits are designed to be sterile when sealed.
Check for kits labeled with model numbers like DYNJ19492L, DYNJ22354L, or others listed in the recall. Look for specific lot numbers such as 24ABE741, 23LBN139, etc., on the packaging.
Look for model numbers and lot numbers on the kit packaging to confirm if it's affected.
Reach out to Medline for assistance with the recall if you have the affected kits.
The kits are safe if the breather pouch seal remains unopened. However, if the seal is opened, non-sterile product may be used, increasing infection risk.
Check the model number and lot number on the kit packaging. Affected kits have specific model numbers like DYNJ19492L and lot numbers such as 24ABE741.
Contact Medline directly for guidance on next steps, as the recall does not specify a return or replacement process.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0178-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0178-2025 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.
