Medline recalls convenience kits with specific syringe packs due to leaks and breakage risks that could harm patients. Learn which kits are affected and what to do.
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 convenience kits containing syringes that may leak or break, posing a risk to patient health. These kits were sold with specific pack numbers and lot numbers between March 2024 and 2025. Affected users should check their kits and contact Medline for a replacement.
The syringes in these kits can leak or break, which may lead to patient health risks such as infection or injury. This issue was identified by the FDA in a safety alert from March 19, 2024.
Healthcare providers and patients using Medline convenience kits with the listed pack numbers and lot numbers are affected. Those handling medical syringes are at higher risk due to potential leaks or breakage.
Check for kits labeled with specific pack numbers like DYNDM1076A or DYNJ45158A, and lot numbers from 19CBP748 to 23IBF733. These kits were sold between March 2024 and 2025.
Look for pack numbers such as DYNDM1076A or DYNJ45158A and lot numbers from 19CBP748 to 23IBF733 on the kit.
Reach out to Medline Industries for a replacement kit if you have the affected items.
The FDA issued a safety alert on March 19, 2024, identifying leaks and breakage risks in these syringes that could harm patients.
Convenience kits with specific pack numbers like DYNDM1076A or DYNJ45158A and lot numbers from 19CBP748 to 23IBF733 are affected.
No, but you should check your kits and contact Medline for a replacement if you have the affected items.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2986-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2986-2024 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.
