Medline recalls 34 procedure kits with plastic syringes that may leak or break, potentially harming patients. Affected kits include Angio Drape Packs and others with specific 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 34 different procedure kits that contain plastic syringes which may leak or break. This 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 or breakage issues. These problems could lead to potential harm to patients during medical procedures.
Healthcare professionals and medical facilities that use these procedure kits are likely affected. Patients receiving procedures using these kits may be at risk if the kits leak or break.
Check for kits labeled with specific names like 'ANGIO DRAPE PACK' or 'ANGIO PACK' and the listed pack numbers (e.g., DYNJ47718D, DYNJ69678). Also look for the lot numbers provided in the recall notice.
Look for the specific product names and pack numbers listed in the recall notice to determine if your kit is affected.
The recall affects 34 different procedure kits from Medline, including Angio Drape Packs and Angio Packs with specific pack numbers like DYNJ47718D and DYNJ69678.
Check the product name and pack number on your kit. Affected kits include those labeled with specific names like 'ANGIO DRAPE PACK' and pack numbers listed in the recall notice.
The recall notice does not specify a remedy, so you should check with Medline directly to determine the next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1437-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1437-2025 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.
