Medline recalls 210+ procedure kits labeled with specific pack numbers for potential leaks, breakage, and quality issues that could affect patient health. 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 210+ medical procedure kits that contain plastic syringes affected by a FDA safety alert. These kits may leak or break, posing a risk to patient health. Affected kits include ACL arthroscopy packs, arteriogram packs, and other surgical kits with specific pack numbers.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, and quality issues. These problems could lead to patient health risks during medical procedures.
Healthcare providers and medical facilities that use Medline procedure kits are likely affected. Patients using these kits during procedures may be at risk if the kits leak or break.
Check for specific pack numbers listed in the recall: ACL ARTHROSCOPY PACK (Pack Numbers DYNJ55316G, DYNJ64332, etc.), ARTERIOGRAM PACK (Pack Number DYNJ64332), and other kits with the listed pack numbers and lot numbers.
Look for specific pack numbers listed in the recall to identify affected kits.
Reach out to Medline for further assistance or to confirm if your kit is affected.
The recall states that these kits may leak or break, posing a risk to patient health. Affected kits should not be used until resolved.
Check for specific pack numbers listed in the recall, such as ACL ARTHROSCOPY PACK (Pack Numbers DYNJ55316G, DYNJ64332, etc.) and ARTERIOGRAM PACK (Pack Number DYNJ64332).
Contact Medline directly to confirm if your kit is affected and follow their instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1465-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1465-2025 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.
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.
