Medline recalls specific procedure kits due to leaks and breakage risks in plastic syringes that could harm patients. Affected kits include GYN, Cysto, and other medical packs with listed pack numbers and lot numbers.
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 several medical procedure kits that contain plastic syringes prone to leaks and breakage. This could pose a risk to patient health if the kits are used as intended.
The plastic syringes in these kits can leak or break, which may lead to patient health risks. This issue was identified through an FDA safety alert from March 19, 2024.
Healthcare providers and medical facilities that use these specific Medline procedure kits are most at risk. Patients using the kits for procedures may also be affected if the syringes leak or break.
Check for kits labeled as L S GYN PACK (Pack Number DYNJ65616C), MAIN CYSTO (Pack Number DYNJ61371A), or other specified packs with the listed lot numbers and pack numbers.
Look for the specific pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall states that leaks and breakage may pose a risk to patient health, so affected kits should not be used until the remedy is completed.
The recall does not specify a remedy, so contact Medline directly for guidance on how to handle the affected kits.
Check the kit label for the specific pack numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1450-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1450-2025 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.
