Merit Medical recalls convenience kits containing Jiangsu Shenli Medical syringes K04 that may leak or break, posing health risks. Affected kits have specific lot numbers and were sold from March 2024.
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.
Merit Medical is recalling convenience kits that include syringes made by Jiangsu Shenli Medical. These syringes may leak or break, which could harm patients during medical use.
The syringes may leak or break during use, which could lead to patient injury or infection. This risk is due to quality issues identified by the FDA in March 2024.
Patients using these kits for medical injections are most at risk. Anyone with the specific lot numbers listed in the recall is affected.
Check for lot numbers H2387533 through H2916432 on the syringe packaging. The kits are labeled as K04 (Custom Syringe Kit) with reference number K04-00791A.
Look for lot numbers H2387533 through H2916432 on the syringe packaging to confirm if the kit is affected.
The FDA identified leaks and breakage risks in these syringes, which could harm patients during medical use.
Check the lot numbers on the syringe packaging. If affected, stop using the kit and contact Merit Medical for further instructions.
The affected syringes were sold from March 2024 with lot numbers H2387533 through H2916432.
We’ve drafted a message you can send Merit Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2561-2024 — Merit Medical Merit Medical Hello, I own a Merit Medical that is covered by recall Z-2561-2024 from Merit Medical. 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.