Medline recalls procedural kits labeled ARTHROGRAPH TRAY with pack number MNS12670A due to leaks and breakage risks that could harm patient health.
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 procedural kits labeled ARTHROGRAPH TRAY with pack number MNS12670A because plastic syringes in these kits may leak or break, posing a risk to patient health. This recall is important because medical devices that cause leaks or breakage could lead to health issues during patient care.
The plastic syringes in these kits may leak or break, which could lead to patient health issues. This risk arises from the quality issues identified in the FDA Safety Alert of March 19, 2024.
Healthcare professionals using Medline procedural kits labeled ARTHROGRAPH TRAY with pack number MNS12670A are most at risk. Patients receiving care with these kits could also be affected if leaks or breakage occur.
Check for kits labeled 'ARTHROGRAPH TRAY' with pack number MNS12670A. The lot number for this specific batch is 2022112990.
Look for the label 'ARTHROGRAPH TRAY' and pack number MNS12670A on the kit.
The plastic syringes in these kits may leak or break, which could pose a risk to patient health as identified in the FDA Safety Alert of March 19, 2024.
Check for kits labeled 'ARTHROGRAPH TRAY' with pack number MNS12670A and lot number 2022112990.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2754-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2754-2024 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.
