Medline recalls procedural kits with specific pack numbers and lot numbers due to potential leaks and breakage of plastic syringes, which could pose health risks to 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 procedural kits that contain plastic syringes prone to leaks and breakage. This could lead to health risks for patients using these kits during medical procedures.
The plastic syringes in these kits may leak or break, potentially causing contamination or injury to patients. This issue was identified following an FDA safety alert in March 2024.
Healthcare professionals and patients using Medline procedural kits with the specified pack numbers and lot numbers are affected. Those handling the kits in medical settings are most at risk.
Check for kits labeled 'SR C SECTION' with pack numbers DYNJ908584 or DYNJ908584A, or 'C SECTION' with pack number DYNJ909098. Look for specific lot numbers listed in the recall notice.
Review the pack number and lot numbers on the kit to determine if it is affected by this recall.
Medline procedural kits labeled 'SR C SECTION' with pack numbers DYNJ908584 or DYNJ908584A, and 'C SECTION' with pack number DYNJ909098, along with specific lot numbers.
The plastic syringes in these kits may leak or break, posing a risk to patient health as identified by the FDA in March 2024.
The recall does not require immediate discontinuation; however, affected kits should be checked and replaced if necessary.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2762-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2762-2024 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.
