Medline recalls 11 medical convenience kits with potential leaks and breakage that could harm patients. Affected kits include venous access trays and dialysis insertion bundles. Consumers should stop using these kits immediately.
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 11 specific medical convenience kits that may leak or break, posing a risk to patient health. These kits are used in healthcare settings and could cause harm if the plastic components fail during medical procedures.
The plastic syringes in these kits can leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is heightened when the kits are used for critical procedures like dialysis or blood draws.
Healthcare professionals and patients using the recalled Medline convenience kits for procedures like venous access or dialysis. Those handling the kits in hospitals or clinics are most at risk.
Check for kits labeled with specific product names and pack numbers listed in the recall, such as VENOUS ACCESS TRAY (Pack Number CVI4830A) or DIALYSIS INSERTION BUNDLE-ADD (Pack Number CVI4835).
Discontinue use of all recalled Medline convenience kits to prevent potential leaks or breakage during medical procedures.
The recall includes 11 specific kits such as VENOUS ACCESS TRAY (Pack Number CVI4830A) and DIALYSIS INSERTION BUNDLE-ADD (Pack Number CVI4835).
Look for the product names and pack numbers listed in the recall, such as VENOUS ACCESS TRAY with Pack Number CVI4830A or DIALYSIS INSERTION BUNDLE-ADD with Pack Number CVI4835.
Stop using the kit immediately to prevent potential leaks or breakage that could harm patients during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3007-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3007-2024 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.
