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. 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 requirements, which could lead to infections during medical procedures.
The ultrasound gel in these kits may not meet sterility standards, meaning it could be contaminated with bacteria or other pathogens. If used during medical procedures, this could lead to infections in patients.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023 are likely affected. Patients using these kits for procedures may be at risk of infection if the gel is not sterile.
Check the product label for model numbers listed in the recall (e.g., DYNJ905151A, DYNJ58346A). The kits were sold by Medline between April 2020 and April 2023 with specific UPC numbers.
Look for model numbers on the kit label, such as DYNJ905151A or DYNJ58346A, to confirm if it's affected.
Reach out to Medline directly for instructions on how to return or replace the affected kits.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Kits with model numbers listed in the recall, such as DYNJ905151A, DYNJ58346A, and others, sold by Medline between April 2020 and April 2023.
Check the product label for the model number and compare it to the list provided in the recall. The kits were distributed between April 2020 and April 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2331-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2331-2023 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.
