Medline recalls 31 convenience kits for eye procedures due to potential weak seals on breather pouches that could lead to contamination. Kits with specific model numbers and lot numbers are affected.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling 31 different convenience kits used in eye procedures because the breather pouches might have weak seals. This could lead to contamination of sterile kits during surgery. Affected users should check their model numbers and lot numbers.
The breather pouches used to package these kits may have open or weak seals. This could allow contamination of the sterile kits during medical procedures, potentially leading to infections or complications.
Healthcare professionals and surgical teams who use Medline convenience kits for eye procedures are most at risk. The recall affects specific model numbers and lot numbers listed in the notice.
Check the model number on the kit (e.g., DYNJ41097A) and the lot number (e.g., 24IBF244) listed in the recall notice. The affected kits are used for various eye procedures and have specific model numbers and lot numbers provided.
Look for the model number (e.g., DYNJ41097A) and lot number (e.g., 24IBF244) on the kit packaging.
The recall includes 31 specific convenience kits for eye procedures with model numbers like DYNJ41097A and lot numbers like 24IBF244.
The breather pouches may have open or weak seals, which could lead to contamination of the sterile kits during medical procedures.
No, the recall does not require immediate discontinuation. Affected users should check their model and lot numbers and contact Medline if needed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1617-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1617-2025 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.
