Medline recalls procedural kits with specific pack numbers due to leaks and breakage risks that could harm patients. Affected kits include carotid endarterectomy packs and PICC insertion trays.
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 certain procedural kits used in medical procedures because plastic syringes in these kits may leak or break, posing a risk to patient health. This recall affects specific pack numbers and lots sold since March 2024.
The plastic syringes in these kits may leak or break, which could lead to patient health issues. This problem was identified following an FDA safety alert from March 19, 2024.
Healthcare professionals and medical facilities using the recalled procedural kits are most at risk. Patients receiving procedures with these kits could be affected if the kits malfunction.
Check for kits labeled as CAROTID ENDARTERECTOMY PK with pack number DYNJ85516 or PICC INSERTION TRAY W/O CATH with pack number PICCNC0004. Also look for specific lot numbers listed in the recall notice.
Look for the product labels and pack numbers listed in the recall notice to confirm if your kit is affected.
The recall includes CAROTID ENDARTERECTOMY PK with pack number DYNJ85516 and PICC INSERTION TRAY W/O CATH with pack number PICCNC0004.
Check the product labels for the specific pack numbers and lot numbers listed in the recall notice.
The recall notice does not specify a remedy, so affected users should check the kit labels and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2745-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2745-2024 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.
