Medline recalls procedure kits with specific pack numbers due to potential leaks and breakage in plastic syringes, which could harm patient health. Affected kits include Laceration Tray Pack Number DYNJ17328B.
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 Laceration Tray with pack number DYNJ17328B because plastic syringes in these kits may leak or break, posing a risk to patient health. This recall is important because medical devices that could cause harm during procedures need to be safe.
The plastic syringes in these kits may leak or break, which could lead to patient health risks. This issue is linked to a FDA safety alert from March 19, 2024, indicating quality problems with the syringes.
Healthcare professionals using Medline procedure kits for medical procedures are most at risk. Patients receiving care during these procedures could be affected if the kits contain faulty syringes.
Check for the Laceration Tray label and pack number DYNJ17328B on the kit. The kit may also have a UDI/DI number 10080196232895 (each) or 40080196232896 (case) and lot number 21LBA554A.
Look for the pack number DYNJ17328B and UDI/DI numbers 10080196232895 or 40080196232896 on the kit.
The recall is due to plastic syringes in the kits potentially leaking or breaking, which could pose a risk to patient health, as noted in a FDA safety alert from March 19, 2024.
The official recall record does not specify a remedy or action steps beyond checking the kit details.
Yes, the affected kits have pack number DYNJ17328B and UDI/DI numbers 10080196232895 (each) or 40080196232896 (case), with lot number 21LBA554A.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1445-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1445-2025 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.
