Medline recalls convenience kits with specific pack numbers and lot numbers due to potential leaks and breakage in plastic syringes, which could pose health risks to patients.
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 labeled as CYSTO PACK with specific pack numbers and lot numbers. These kits contain plastic syringes that may leak or break, posing a risk to patient health.
The plastic syringes in these kits can leak or break, potentially causing contamination or injury to patients. This issue is linked to a FDA safety alert from March 19, 2024, indicating quality problems with the syringes.
Healthcare professionals and patients who use these convenience kits are likely affected. Those handling the kits with the specified pack numbers and lot numbers are at the highest risk.
Check for CYSTO PACK kits with pack numbers DYNJ42742D or DYNJ42799. Look for specific lot numbers listed in the recall notice to identify affected units.
Identify the pack number and lot number on the kit to determine if it is affected by this recall.
The recall is due to potential leaks and breakage in the plastic syringes, which could pose a risk to patient health as identified by a FDA safety alert from March 19, 2024.
The official recall notice does not specify a remedy, so check the product details to see if it is affected and contact Medline for further instructions.
Affected kits have specific pack numbers (DYNJ42742D or DYNJ42799) and the listed lot numbers. Check the product label for these details.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3013-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3013-2024 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.
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.
