Medline recalls General Endoscopy Packs with Pack Number DYNJ44673G due to potential leaks and breakage in syringes 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 kits labeled as General Endoscopy Packs with Pack Number DYNJ44673G. These kits contain plastic syringes that may leak or break, posing a risk to patient health.
The plastic syringes in these kits may leak or break, which could lead to patient health issues. This risk is related to the FDA Safety Alert from March 19, 2024.
Healthcare providers using these kits for medical procedures are most at risk. Patients receiving care from these kits could be affected if the syringes leak or break.
Check for General Endoscopy Packs labeled with Pack Number DYNJ44673G. The kits may have UDI/DI numbers 10195327127473 (each) and 40195327127474 (case), Lot Number 22KDC145A.
Look for the Pack Number DYNJ44673G on the label of the General Endoscopy Pack.
The product is recalled due to potential leaks and breakage in plastic syringes that could pose a risk to patient health, as noted in an FDA Safety Alert from March 19, 2024.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the product.
The recalled product is labeled as General Endoscopy Packs with Pack Number DYNJ44673G, UDI/DI numbers 10195327127473 (each) and 40195327127474 (case), and Lot Number 22KDC145A.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1442-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1442-2025 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.
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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.
