Medline recalls CV Neonatal Procedure Kits with Pack Number DYNJ67356 due to potential leaks and breakage that could harm patients. Affected kits may need replacement.
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 kits labeled 'CV NEONATAL PACK' with specific pack numbers because they may leak or break, posing a risk to patient health. This recall is important for healthcare providers using these kits to avoid potential harm.
These kits contain plastic syringes that can leak or break, potentially causing harm to patients. The issue is linked to a FDA safety alert from March 2024, indicating quality problems with the syringes.
Healthcare providers using Medline CV Neonatal Procedure Kits with Pack Number DYNJ67356 are likely affected. Patients receiving care from these kits may be at risk if the kits leak or break.
Check for the CV NEONATAL PACK label and Pack Number DYNJ67356 on the kit. The kits also have a UDI/DI code 10193489887136 (each) and 40193489887137 (case), with Lot Number 23GMF016A.
Look for the CV NEONATAL PACK label and Pack Number DYNJ67356 on the kit.
Medline CV Neonatal Procedure Kits with Pack Number DYNJ67356.
The kits contain plastic syringes that may leak or break, posing a risk to patient health as noted in a FDA safety alert from March 2024.
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-1443-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1443-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
