Medline recalls 70+ medical convenience kits due to plastic syringe leaks and breakage that may harm patients. Affected kits include specific pack numbers and lot numbers listed in the recall. No remedy provided in official notice.
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 over 70 medical convenience kits that contain plastic syringes with potential leaks and breakage risks. This could pose a health hazard to patients during medical procedures. Affected kits have specific pack numbers and lot numbers listed in the recall notice.
The recall is based on FDA safety alerts identifying leaks and breakage in plastic syringes within these kits. These issues could lead to patient health risks if the syringes are used improperly or if they cause contamination.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using the kits during procedures may be exposed to potential health hazards.
Check for specific pack numbers listed in the recall, such as MYELOGRAM PACK (Pack Number 00-399025L), BIOPSY PROCEDURE PACK (Pack Number 00-399227G), and other kits with their corresponding lot numbers. The recall covers 70+ different kit types.
Identify if your kit matches the specific pack numbers and lot numbers listed in the recall notice.
The recall is due to FDA safety alerts identifying leaks and breakage in plastic syringes within these kits, which could pose a risk to patient health.
The official notice does not provide a remedy. You should check if your kit matches the listed pack numbers and lot numbers to determine if it's affected.
The recall covers 70+ different medical convenience kits with specific pack numbers and lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3019-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3019-2024 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.
