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 the kits may not meet sterility specifications, meaning it could be contaminated. This contamination risk might lead to infections during medical procedures if the gel is used improperly.
Medical professionals and healthcare facilities that use these kits for procedures like biopsies or drainage. The risk is low as the issue relates to potential sterility failures, not immediate safety hazards.
Check the model numbers and UPCs listed in the recall notice. Affected kits were sold by Medline between April 2020 and April 2023. The specific model numbers and UPCs are detailed in the recall document.
Look for the model numbers and UPCs listed in the recall notice to confirm if your kit is affected.
The ultrasound gel in the kits may not meet sterility specifications, which could lead to contamination and potential infections during medical procedures.
Kits with model numbers and UPCs listed in the recall notice, sold by Medline between April 2020 and April 2023.
No, the recall does not require immediate discontinuation. The hazard is low risk related to potential sterility failures, not immediate safety hazards.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2307-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2307-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
