Medline recalls 62 procedural kits with plastic syringes that may leak or break, posing health risks. Check pack numbers and lot numbers listed to see if your kit is affected.
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 62 different procedural kits that contain plastic syringes which may leak or break, potentially causing health risks. These kits are used in medical procedures and should be checked for the specific pack numbers and lot numbers listed in the recall.
The plastic syringes in these kits have been identified as leaking or breaking, which could lead to health risks for patients during medical procedures. This issue was noted in an FDA safety alert from March 19, 2024.
Healthcare professionals and medical facilities that use Medline procedural kits are most at risk. Patients using these kits during procedures may be affected if the syringes leak or break.
Check the pack number and lot number on the kit. Affected kits include specific models like OPEN HEART PEDS (Pack Number CDS981050Q) with lot numbers such as 23IBJ172.
Look for the pack number and lot number on the kit to determine if it's affected by this recall.
The recall includes 62 specific procedural kits with pack numbers like CDS981050Q, CDS982411N, and others, each with specific lot numbers.
No, but you should check the pack number and lot number to see if your kit is affected. If it is, you may need to replace it.
The recall does not specify a remedy, so you should contact Medline directly to get guidance on replacing the 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-2743-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2743-2024 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.
