Medline recalls procedure packs containing Shenli syringes that may leak or break, posing health risks. Affected kits include Dialysis Cath Access Kit 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 procedure packs that contain Shenli syringes which may leak or break, potentially harming patients. This recall affects specific kits used in dialysis treatments.
The syringes in these procedure packs have been identified by the FDA as having leaks and breakage issues. These problems could lead to patient health risks during dialysis treatments.
Healthcare workers using dialysis procedure kits are most at risk. Patients receiving treatments with these kits could be affected if the syringes leak or break.
Check for procedure packs labeled as Dialysis Cath Access Kit, Dialysis Pack, Dialysis AV Shunt, Dialysis Access Pack, or No Cath Dialysis Insertion Tray. Look for specific pack numbers and lot numbers listed in the recall notice.
Look for the specific pack numbers and lot numbers listed in the recall notice to identify affected items.
The FDA identified leaks and breakage issues in Shenli syringes used in these procedure packs, which could pose a risk to patient health.
Procedure packs labeled as Dialysis Cath Access Kit (Pack Number DYNDA2516B), Dialysis Pack (Pack Number DYNJ36932A), Dialysis AV Shunt #668229-V-LF, Dialysis Access Pack (Pack Number DYNJ910121), and No Cath Dialysis Insertion Tray (Pack Number PICCNC0028) with specific lot numbers.
The recall does not specify a stop-use instruction; affected products should be checked for the listed pack numbers and lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2630-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2630-2024 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.
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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.
