Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were distributed between April 2020 and April 2023. Consumers should check model numbers and UPCs listed in the recall.
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 specifications, which could lead to infections during medical procedures.
The ultrasound gel in these kits may not meet sterility standards, potentially leading to contamination and infection during medical procedures. This is a risk for procedures requiring sterile environments.
Healthcare professionals and medical facilities that use these kits for procedures. Patients undergoing procedures with these kits may be at risk of infection.
Check the model numbers and UPCs listed in the recall. Affected kits were distributed between April 2020 and April 2023. The kits are labeled as ANGIO, ANGIO BASIN SET, and other specific product names.
Look for model numbers and UPCs listed in the recall to determine if your kit is affected.
Reach out to Medline directly for assistance with the recall process.
The ultrasound gel in these kits may not meet sterility specifications, potentially leading to contamination and infection during medical procedures.
Check the model numbers and UPCs listed in the recall. Affected kits were distributed between April 2020 and April 2023.
No, the recall does not require immediate discontinuation. However, you should check if your kit is affected and contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2296-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2296-2023 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.
