Medline recalls 23 medical convenience kits with potential leaks and breakage that could harm patients. Affected kits include infection driveline management kits and PICU line trays. Contact Medline for details.
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 23 different medical convenience kits that may leak or break, posing a risk to patient health. These kits include infection driveline management kits and PICU line trays. If you have any of these kits, stop using them immediately to prevent potential harm.
The kits contain plastic syringes that may leak or break due to quality issues. This can lead to patient health risks such as infections or injuries if the kits are used improperly.
Healthcare professionals and hospitals that use Medline convenience kits are most at risk. Patients receiving care with these kits could be harmed if leaks or breakage occur.
Check for kits labeled with specific pack numbers like DM645, DYNDC1960A, or SPEC0095. Look for lot numbers such as 2019120980 or 2022040790 on the packaging.
Discontinue use of all recalled Medline convenience kits to prevent potential leaks or breakage that could harm patients.
The recall includes 23 specific medical convenience kits such as infection driveline management kits (Pack Number DM645) and PICU line trays (Pack Number DYNDC1960A).
Check the pack number and lot number on the kit's packaging. Affected kits have specific pack numbers like DM645 or DYNDC1960A and lot numbers such as 2019120980 or 2022040790.
Stop using the kit immediately and contact Medline for further instructions on disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3029-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3029-2024 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.
