Merit Medical recalls convenience kits containing syringes from Jiangsu Shenli Medical that may leak or break, posing health risks. Affected kits include specific catalog 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.
Merit Medical is recalling convenience kits that contain syringes made by Jiangsu Shenli Medical. These syringes may leak or break, which could harm patients during medical treatments.
The syringes in the kits can leak or break during use, potentially causing infections or other health issues for patients receiving medical treatments. This risk is due to quality issues identified by the FDA in March 2024.
Patients using these convenience kits for medical fluid administration are at risk. Healthcare providers and individuals with medical devices that use these syringes may also be affected.
Check for convenience kits with catalog numbers K08-02042, K08-02948, K08-03026, or K08-03119. Look for specific lot numbers listed in the recall notice.
Identify the catalog number and lot numbers on your convenience kit to confirm if it is affected.
Reach out to Merit Medical for assistance with the recall process or to get replacement kits.
The FDA issued a safety alert in March 2024 that these syringes may leak or break, posing a risk to patient health.
Check the catalog number and lot numbers on your kit to see if it is affected. Contact Merit Medical for further instructions.
Affected kits have specific catalog numbers (K08-02042, K08-02948, K08-03026, K08-03119) and listed lot numbers.
We’ve drafted a message you can send Merit Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2563-2024 — Merit Medical Merit Medical Hello, I own a Merit Medical that is covered by recall Z-2563-2024 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.
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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.
