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 specifications, meaning it could be contaminated. This contamination risk could lead to infections during medical procedures if the gel is used in sterile environments.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is highest for those using the kits in sterile environments where contamination could cause infections.
Check the model numbers and UPCs listed in the recall notice. Products distributed by Medline between April 2020 and April 2023 with specific model numbers (e.g., ECVC4740, DYNJ36212C) are affected.
Identify the model number and UPC code on the kit to confirm if it is in the recall list.
Custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel with model numbers and UPCs listed in the recall notice, distributed by Medline between April 2020 and April 2023.
Check the model number and UPC code on the kit. The recall includes specific model numbers (e.g., ECVC4740) and UPCs distributed between April 2020 and April 2023.
Check the product details to confirm if it is in the recall list. If it is, contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2319-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2319-2023 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.
