Medline recalls anesthesia turnover kits with non-sterile Mastisol 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 certain anesthesia turnover kits because they contain a non-sterile Mastisol component that wasn't properly labeled. This increases the risk of patient infection if the user assumes the kit is sterile during use.
The kit contains a non-sterile Mastisol component that was not labeled as sterile or non-sterile. If healthcare workers assume the entire kit is sterile during use, it could lead to patient infections.
Healthcare professionals using the recalled anesthesia turnover kits are most at risk. Patients receiving procedures with these kits could face infection if the kit is not handled with proper sterility.
Check for the pack number DYNJAA0377A on the kit. The lot numbers include 23IBJ309, 23GBA500, 23GBA457, 23CBE394, and 23BBL312.
Look for the pack number DYNJAA0377A and lot numbers listed above on the kit.
The kit contains a non-sterile Mastisol component that wasn't labeled as sterile or non-sterile, increasing the risk of patient infection if used without proper sterility checks.
Check the kit label for the pack number DYNJAA0377A and lot numbers. If you have the recalled kit, contact Medline for guidance.
The recall addresses a risk of patient infection, not physical injury. The hazard is specific to sterility and does not involve immediate physical harm.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-3072-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-3072-2024 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.
