Medline recalls Neuro Angio Pack procedure kits with Shenli syringes (Pack # DYNDA1431A, Lot # 2020012890) 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 labeled 'NEURO ANGIO PACK' with Shenli syringes (Pack Number DYNDA1431A) because leaks and breakage may harm patients. This affects medical kits used in healthcare settings.
The syringes in these procedure packs may leak or break, potentially causing patient injuries. This risk is linked to a FDA safety alert from March 2024 about quality issues with the syringes.
Healthcare providers using Medline procedure packs labeled 'NEURO ANGIO PACK' with Pack Number DYNDA1431A are most at risk. Patients using these kits could face health issues from syringe leaks or breakage.
Check for procedure packs labeled 'NEURO ANGIO PACK' with Pack Number DYNDA1431A and Lot Number 2020012890. These kits were sold by Medline Industries, LP in Northfield.
Look for the label 'NEURO ANGIO PACK' with Pack Number DYNDA1431A and Lot Number 2020012890 on the syringe kit.
The FDA issued a safety alert in March 2024 about leaks and breakage risks with these syringes, which could harm patients.
Check for procedure packs labeled 'NEURO ANGIO PACK' with Pack Number DYNDA1431A and Lot Number 2020012890.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2633-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2633-2024 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.
