Medline recalls procedure packs containing Shenli syringes (model ECVC8105, ECVC8045) due to leaks and breakage risks that could harm patients. Affected units include specific pack numbers and lot dates.
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 during medical procedures. This recall affects specific pack numbers and lot dates listed in the notice.
The Shenli syringes in these packs may leak or break during use, potentially causing patient injury. This issue is linked to a FDA safety alert from March 19, 2024, which identified quality problems with the syringes.
Healthcare workers and patients using Medline procedure packs with Shenli syringes (models ECVC8105 and ECVC8045) are affected. Those using the recalled packs with specific lot numbers are at the highest risk.
Check for packs labeled 'CVC DOUBLE LUMEN 16CM' (Pack Number ECVC8105) or 'VANTEX 7FR 3L 20CM CVC BUNDLE US' (Pack Number ECVC8045). The affected units have specific lot numbers: 2023052690, 2023100490, or 2023110990.
Look for Pack Numbers ECVC8105 or ECVC8045 on the procedure packs.
Ensure the lot numbers match the affected ones: 2023052690, 2023100490, or 2023110990.
The recalled packs contain Shenli syringes labeled as CVC DOUBLE LUMEN 16CM (Pack Number ECVC8105) or VANTEX 7FR 3L 20CM CVC BUNDLE US (Pack Number ECVC8045).
Yes, the affected units have lot numbers 2023052690, 2023100490, or 2023110990.
The recall record does not specify a remedy, so check with Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2631-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2631-2024 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.
