Medline recalls 26 procedural kits with plastic syringes that may leak or break, posing patient health risks. Affected kits include circumcision trays and sterile syringes with specific pack numbers and lot numbers.
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 26 different procedural kits that contain plastic syringes which may leak or break, potentially causing health risks to patients. These kits are used in medical settings for procedures like circumcision and biopsies.
The plastic syringes in these kits have been identified by the FDA as having leaks or breakage issues. This could lead to patient health risks if the syringes fail during medical procedures.
Healthcare providers and medical facilities that use these specific Medline procedural kits are most at risk. Patients using these kits during procedures could be affected if the syringes leak or break.
Check for kits labeled with specific product names like ARTHROGRAM TRAY, CIRCUMCISION TRAY, or STERILE 1CC SYR, along with the pack numbers and lot numbers listed in the recall notice.
Identify the product name and pack number from the recall list to confirm if your kit is affected.
The recall states that these kits may have leaks or breakage issues, so they are not safe to use until replaced with unaffected kits.
Check the product name and pack number against the list provided in the recall notice, which includes specific kits like ARTHROGRAM TRAY with pack number MNS11965A.
The recall does not specify a remedy, so contact Medline directly for guidance on how to handle affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2752-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2752-2024 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.
