Medline recalls angiography procedure kits with specific pack numbers and UDI/DI codes due to potential leaks and breakage 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 angiography procedure kits that contain plastic syringes with possible leaks or breakage. This could pose a risk to patient health during medical procedures.
The plastic syringes in these kits can leak or break, potentially causing harm to patients during medical procedures. This issue was identified through a FDA safety alert from March 19, 2024.
Healthcare professionals using Medline angiography procedure kits with pack number DYNJ60655D and UDI/DI codes 10195327464783 or 40195327464784 are most at risk. Patients receiving these kits during medical procedures may also be affected.
Check for the pack number DYNJ60655D and UDI/DI codes 10195327464783 (each) or 40195327464784 (case) on the kit label. These kits were sold with lot number 24AMC692A.
Look for pack number DYNJ60655D and UDI/DI codes 10195327464783 or 40195327464784 on the kit label.
The plastic syringes in these kits can leak or break, potentially causing harm to patients during medical procedures, as identified by a FDA safety alert from March 19, 2024.
Check the kit label for pack number DYNJ60655D and UDI/DI codes 10195327464783 or 40195327464784. If you have these, contact Medline for further instructions.
The recall notice does not specify a deadline for action.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1463-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1463-2025 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.
