Merit Medical recalls convenience kits containing Jiangsu Shenli Medical syringes K11-00382C due to leaks and breakage risks that could harm patients during medical procedures.
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 cause harm to patients during medical procedures.
The syringes in these kits can leak or break during use, potentially causing injury or infection to patients. This risk is especially concerning during medical procedures where precise fluid administration and pressure monitoring are needed.
Patients using these kits for medical procedures like blood pressure monitoring or cardiac interventions are most at risk. Healthcare providers who use the kits for clinical purposes may also be affected.
Check for the model K11-00382C on the kit label. The kits were sold with specific lot numbers including 00884450158425, H2379628, H2531736, H2536619, H2813488, H2881603, H2916468.
Look for the model number K11-00382C on the convenience kit label to confirm if it's affected.
Reach out to Merit Medical for guidance on next steps if the kit is confirmed affected.
The syringes in these kits may leak or break, which could cause harm to patients during medical procedures.
Check the kit label for model K11-00382C. If affected, contact Merit Medical for guidance.
Yes, affected kits include lot numbers 00884450158425, H2379628, H2531736, H2536619, H2813488, H2881603, H2916468.
We’ve drafted a message you can send Merit Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2566-2024 — Merit Medical Merit Medical Hello, I own a Merit Medical that is covered by recall Z-2566-2024 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.
