Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Kits labeled with specific pack numbers and lot numbers are affected. Consumers should check their kits and contact Medline for details.
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 convenience kits that contain plastic syringes which may leak or break, potentially causing health risks to patients. These kits were distributed with specific pack numbers and lot numbers identified in the recall.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, or quality issues that could pose a risk to patient health during medical procedures.
Healthcare professionals and patients using these kits for medical procedures are most at risk. The kits are used in catheter labs and other medical settings.
Check for kits labeled with specific pack numbers like 'CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O' or similar. The kits include various medical trays and components with specific lot numbers.
Look for specific pack numbers and lot numbers listed in the recall to determine if your kit is affected.
Medline is recalling convenience kits that contain plastic syringes with potential leaks or breakage, which could pose health risks during medical procedures.
Check the kit label for specific pack numbers and lot numbers listed in the recall, such as 'CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O' or similar.
The recall does not specify a remedy, so you should check your kit label to see if it matches the affected pack numbers and lot numbers listed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2993-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2993-2024 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.
