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. 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 if used in medical procedures. This recall affects kits distributed between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, meaning it could be contaminated. If used in medical procedures, this could lead to infections or other complications, but the risk is not immediate or severe under normal use.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is low for most users since the hazard is related to sterility standards, not immediate injury.
Check the model numbers and UPCs listed in the recall notice. Affected kits were distributed by Medline between April 2020 and April 2023. The kits include specific procedural kits with Turkuaz ultrasound gel.
Review the model numbers and UPCs listed in the recall notice to confirm if your kit is affected.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used in medical procedures.
Check the model numbers and UPCs listed in the recall notice. Affected kits were distributed by Medline between April 2020 and April 2023.
No, the recall is for sterility concerns, not immediate safety risks. However, you should check if your kit is affected before use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2299-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2299-2023 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.
