Medline recalls certain sterile convenience kits due to non-sterile components that could cause patient infections if used without proper sterility checks.
A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
Medline is recalling specific sterile convenience kits because they contain non-sterile components that may lead to infections if the user mistakenly assumes the kit is sterile. This affects patients who use these kits for medical procedures.
The kits contain non-sterile components that were mistakenly placed in the non-sterile portion of the sterile kits. If users believe the kit is sterile, they could introduce infections during medical procedures.
Patients using the recalled sterile convenience kits for medical procedures are at risk of infection if they assume the kit is sterile when it is not. Healthcare providers who use these kits should check the lot numbers.
Check for the pack number DYNJ907372A on the kit. The lot numbers include 23ILA372, 23ILA184, and other specific numbers listed in the recall notice.
Look for the lot numbers listed in the recall: 23ILA372, 23ILA184, 23HLB240, 23HLA567, 23HLA126, 23ELA634, 23DLA974, 23ALA995, 22JLA577, 22HLA985, 22HLA379, 22GLB224, 22GLB099, 22GLA383, 22GLA171, 22DLA615, 22CLA957, 22ALA965, 22ALA325.
The kits contain non-sterile components that were mistakenly placed in the non-sterile portion of the sterile kits, increasing the risk of patient infection if the user assumes sterility.
Check the pack number DYNJ907372A and the lot numbers listed: 23ILA372, 23ILA184, 23HLB240, 23HLA567, 23HLA126, 23ELA634, 23DLA974, 23ALA995, 22JLA577, 22HLA985, 22HLA379, 22GLB224, 22GLB099, 22GLA383, 22GLA171, 22DLA615, 22CLA957, 22ALA965, 22ALA325.
The recall does not specify a remedy, so you should check with Medline Industries to determine if you need to discard or return the kit.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-3070-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-3070-2024 from Medline Industries. 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.
