Medline recalls 69 procedure kits with plastic syringes that may leak or break, posing health risks. Kits labeled with specific pack numbers and lot numbers are affected. Contact Medline for details.
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 69 different procedure kits that contain plastic syringes with potential leaks or breakage. These issues could pose a risk to patient health during medical procedures.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, or quality issues that could pose a risk to patient health during medical procedures.
Healthcare professionals and patients using these procedure kits for medical procedures are likely affected. The risk is primarily for those using the kits in clinical settings.
Check the product label for specific pack numbers listed in the recall (e.g., DYNJ40629B, DYNJ67756A) and lot numbers (e.g., 21EME542A).
Look for the pack number and lot number on the label to confirm if your kit is affected.
The recall states that these kits may have leaks or breakage, so they are not safe to use without checking the recall list.
Check the product label for the specific pack number and lot number listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1441-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1441-2025 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.