Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility specifications. Affected kits were distributed between April 2020 and April 2023. Contact Medline for details.
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. Affected kits were sold between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, meaning it could be contaminated. This contamination could lead to infections during medical procedures if the gel is used improperly.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023 are likely affected. Patients using these kits during procedures may be at risk of infection if the gel is not sterile.
Check for kits labeled with model numbers listed in the recall, such as CDS840451L, DYNJ908179, or DYNJ43741B. These kits were distributed by Medline between April 2020 and April 2023.
Look for model numbers like CDS840451L, DYNJ908179, or DYNJ43741B on the kit packaging.
Reach out to Medline Industries for assistance with the recall and to get replacement kits if needed.
The recall states that the ultrasound gel may not meet sterility specifications, so they are not safe for use without replacement.
Check the model number on the kit packaging. Affected kits include models like CDS840451L, DYNJ908179, and DYNJ43741B, distributed between April 2020 and April 2023.
Contact Medline Industries for details on how to get a replacement or return the kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2302-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2302-2023 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.
