Medline recalls procedure packs containing Shenli syringes (part numbers DYNDA1431A, ECVC3260, etc.) due to leaks and breakage risks that could harm patients.
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, potentially causing harm to patients. This recall affects specific medical kits used in healthcare settings.
The Shenli syringes in these packs can leak or break, which may lead to patient injuries or health risks. This issue stems from quality problems identified by the FDA in March 2024.
Healthcare workers and patients using Medline procedure packs with Shenli syringes are affected. Those handling the recalled kits, especially in medical settings, are at higher risk.
Check for procedure packs labeled as NEURO ANGIO PACK (part number DYNDA1431A) or other kits with specific part numbers listed in the recall notice. The kits were sold with certain lot numbers from 2019 to 2023.
Look for the part numbers DYNDA1431A, ECVC3260, ECVC7440, ECVC7445, or ECVC7445A on the packaging.
Reach out to Medline directly to confirm if your specific kit is affected and get instructions for next steps.
The FDA issued a safety alert in March 2024 about leaks and breakage in Shenli syringes, which could pose risks to patient health.
Procedure packs labeled NEURO ANGIO PACK (part number DYNDA1431A) and other kits with specific part numbers like ECVC3260, ECVC7440, ECVC7445, and ECVC7445A are affected.
Check the product labels for the part numbers listed in the recall. Contact Medline for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2632-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2632-2024 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.
