Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were distributed between April 2020 and April 2023.
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Medline is recalling custom sterile and non-sterile procedural kits that contain Turkuaz ultrasound gel. The gel may not meet sterility specifications, which could lead to infections during medical procedures.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used in medical procedures. However, the recall does not specify that the kits are currently causing injuries.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is low because the hazard is related to sterility standards, not immediate harm.
Check the product label for model numbers listed in the recall (e.g., DYNJ40629B, DYNJ81410B). The kits were distributed by Medline between April 2020 and April 2023.
Look for model numbers on the kit label, such as DYNJ40629B or DYNJ81410B, to determine if it is affected.
The recall states the gel may not meet sterility specifications, but it does not mention injuries or deaths. The risk is low and related to potential infections during procedures.
Check the model number on the kit label. Affected kits have model numbers listed in the recall (e.g., DYNJ40629B) and were distributed by Medline between April 2020 and April 2023.
The recall does not specify a remedy, so contact Medline directly to confirm if your kit is affected and get guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2312-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2312-2023 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.
