Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were sold between April 2020 and April 2023 with specific model numbers and UPCs listed.
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 standards, which could lead to infections during medical procedures.
The ultrasound gel in these kits may not meet sterility specifications, meaning it could be contaminated. This contamination risk could lead to infections during medical procedures if the gel is used improperly.
Healthcare professionals and medical facilities that use these kits for procedures. Patients undergoing procedures with these kits are at risk of infection due to potential contamination.
Check for model numbers listed in the recall notice, such as DYNJ61099B, DYNJ61099C, and others. These kits were sold between April 2020 and April 2023 with specific UPC numbers.
Look for model numbers like DYNJ61099B, DYNJ61099C, or others listed in the recall notice to confirm if your kit is affected.
The recall states the gel may not meet sterility specifications, so they are not safe to use without checking the model numbers and UPCs listed in the recall.
Check the model number on your kit against the list of affected models and UPCs provided in the recall notice, which were distributed between April 2020 and April 2023.
The recall does not specify a remedy, so you should contact Medline directly to determine next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2298-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2298-2023 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.
