Medline recalls custom sterile and non-sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility specifications. Affected kits were sold between April 2020 and April 2023. Consumers should check model numbers and UPCs listed in the recall notice.
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. This recall affects kits sold between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used during medical procedures. This is a quality control issue that does not pose an immediate risk of injury or death.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is low as the hazard involves potential sterility issues rather than immediate injury or death.
Check the model numbers and UPCs listed in the recall notice. Affected kits were sold between April 2020 and April 2023. The model numbers include DYNJ65963A, PAIN1524B, and others as detailed in the recall.
Look for the model number on the kit packaging or label to determine if it is affected.
Reach out to Medline customer service for assistance with returns or replacements if the kit is affected.
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 on your kit. Affected kits were sold between April 2020 and April 2023 with specific model numbers listed in the recall notice.
No, the recall is for potential sterility issues, not an immediate risk of injury or death. You can continue using the kits but should check if they are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2338-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2338-2023 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.
