Medline recalls 31 types of eye and surgery kits due to plastic syringe leaks and breakage that may harm patients during medical procedures.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medline is recalling 31 different procedure kits used in eye and surgery treatments because plastic syringes in these kits can leak or break, potentially causing harm to patients during medical procedures.
The plastic syringes in these kits can leak or break, which may lead to patient injuries during medical procedures. This risk is related to the FDA Safety Alert from March 19, 2024.
Healthcare providers and medical facilities that use Medline procedure kits for eye and surgical treatments are most at risk. Patients using these kits during procedures may be affected if the kits leak or break.
Check for Medline procedure kits labeled with specific pack numbers listed in the recall notice. The kits include various eye and surgery packs with unique pack numbers like DYNJ0589795V, DYNJ39921B, and others.
Look for the specific pack numbers listed in the recall notice to identify affected kits.
The FDA Safety Alert from March 19, 2024 identified that plastic syringes in these kits can leak or break, posing a risk to patient health during medical procedures.
Check the pack number on the kit label against the list of affected pack numbers provided in the recall notice.
The recall does not specify a stop-use action; affected kits should be checked and replaced if necessary.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1451-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1451-2025 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.
