Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility specifications. Products distributed between April 2020 and April 2023 with specific model numbers and UPCs are affected.
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 requirements. This could lead to infections if the gel is used during medical procedures where sterility is critical.
Healthcare professionals and medical facilities that use these kits for procedures. Patients undergoing procedures with these kits may be at risk of infection.
Check for model numbers listed in the recall (e.g., DYNJ67517, DYNJ51416B) and UPC numbers provided. Products distributed between April 2020 and April 2023 are affected.
Review the model number and UPC code on the kit to see if it matches the list provided in the recall.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check the model number and UPC code on the kit. Products distributed between April 2020 and April 2023 with the specific model numbers listed in the recall are affected.
No. The recall is for products that may not meet sterility standards, but there is no immediate need to stop using them. Check the model numbers and UPCs to confirm if your product is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2320-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2320-2023 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.
