Medline recalls certain anesthesia turnover 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 anesthesia turnover kits because they contain non-sterile components that could lead to patient infections if the user mistakenly assumes the kit is sterile. This affects healthcare providers using these kits during patient procedures.
The kit contains a non-sterile Mastisol component that was incorrectly placed in the non-sterile section of the kit. If healthcare workers assume the kit is sterile when it isn't, there's a risk of patient infection during medical procedures.
Healthcare professionals who use Medline anesthesia turnover kits with the specified pack number and lot numbers are most at risk. Patients receiving procedures using these kits could face infection risks if the kit is not properly sterilized.
Check for the pack number DYNJAA0377 and lot number 22LBM357 on the anesthesia turnover kit. These kits were distributed by Medline Industries in Northfield, LP.
Verify the pack number and lot number on the kit to confirm if it's affected.
The recall indicates a risk of patient infection if the kit is used without proper sterility checks, but the hazard is not immediately life-threatening.
Look for the pack number DYNJAA0377 and lot number 22LBM357 on the anesthesia turnover kit.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-3071-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-3071-2024 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.
