Medline recalls procedure packs containing Shenli syringes due to leaks and breakage risks. Affected packs have specific pack and lot numbers. Stop using immediately to prevent patient health risks.
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 include Shenli syringes because these syringes may leak or break, which could harm patients. This recall affects specific packs with labeled numbers and dates.
Shenli syringes in these packs may leak or break, leading to potential patient health risks. This issue was identified through an FDA safety alert from March 19, 2024.
Healthcare workers using Medline procedure packs with Shenli syringes are most at risk. Patients receiving care with these syringes could be affected if the syringes leak or break.
Check for packs labeled 'CVC INSERT BUNDLE 16CM' (Pack Number ECVC3260) or 'VANTEX 7FR 3L 20CM CVC BUNDLE US' (Pack Number ECVC8045). The lot numbers are 2018052950 and 2023110290 respectively.
Immediately stop using any procedure packs containing Shenli syringes with the specified pack and lot numbers.
Packs labeled 'CVC INSERT BUNDLE 16CM' (Pack Number ECVC3260) or 'VANTEX 7FR 3L 20CM CVC BUNDLE US' (Pack Number ECVC8045) with lot numbers 2018052950 and 2023110290 respectively.
Shenli syringes may leak or break, which could pose a risk to patient health as identified by an FDA safety alert from March 19, 2024.
Check for the specific pack labels and lot numbers mentioned in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2629-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2629-2024 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.
