Medline Industries recalls 107 batches of breather pouches used in sterile convenience kits due to potential open/weak seals that could compromise sterility.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline Industries is recalling 107 specific batches of breather pouches used for packaging sterile medical kits because some pouches have weak seals that could allow contamination. This affects medical users who have these specific batches.
The breather pouches used for packaging sterile medical kits may have open or weak seals, which could allow contaminants to enter the sterile packaging and compromise the medical kits' sterility. This is a potential contamination risk but not an immediate safety hazard.
Medical professionals and healthcare facilities that use these breather pouches for sterile convenience kits. The risk is low as the hazard is a potential seal issue rather than a direct safety hazard.
Check the product label for the model number (e.g., DYNJ61594, DYNJ31798D) and lot number (e.g., 24IBF062). The recall includes 107 specific batches of breather pouches.
Look for the model number (e.g., DYNJ61594) and lot number (e.g., 24IBF062) on the breather pouch packaging.
The recall is due to potential open or weak seals on the breather pouches that could compromise sterility of the medical kits they package.
Check the product label for the model number (e.g., DYNJ61594) and lot number (e.g., 24IBF062) as listed in the recall notice.
The recall notice does not specify a remedy, so contact Medline Industries for guidance on next steps.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1618-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1618-2025 from Medline Industries. 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.
