Medline recalls sterile eye packs with open seals that may cause contamination during medical procedures. Affected units have specific reference numbers and lot codes. Consumers should check their product details to determine if they are affected.
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
Medline is recalling sterile eye packs that may have open seals, which could lead to contamination during medical procedures. This recall affects specific model numbers and lot codes identified in the notice.
Sterile eye packs with open seals may not maintain their sterility, increasing the risk of contamination during medical procedures. This could potentially lead to infections if the packs are used without proper sterility.
Healthcare professionals using sterile eye packs for medical procedures are most at risk. The recall applies to specific model numbers and lot codes sold under the reference numbers DYNJ37743D and DYNJ37743F.
Check for reference numbers DYNJ37743D or DYNJ37743F on the packaging. Affected units have specific lot numbers: 25EMI333 for DYNJ37743D and 25GMD927 for DYNJ37743F.
Look for reference numbers DYNJ37743D or DYNJ37743F on the packaging to determine if your product is affected.
The eye packs may have open seals, which could lead to contamination during medical procedures.
The affected models are DYNJ37743D and DYNJ37743F with specific lot numbers: 25EMI333 and 25GMD927.
The recall does not require stopping use immediately; check the product details to see if your unit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0510-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0510-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
