Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility specifications. Products distributed between April 2020 and April 2023 are affected. Check model numbers and UPCs listed for affected items.
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.
The ultrasound gel in these kits may not meet sterility specifications, meaning it could be contaminated. This contamination could lead to infections during medical procedures if the gel is used improperly.
Healthcare professionals and medical facilities that use these kits for procedures are most at risk. Patients undergoing procedures with these kits could face infection risks.
Check the model numbers and UPCs listed in the recall notice. Products distributed by Medline between April 2020 and April 2023 are affected. The kits are labeled as VASCULAR or other specific medical procedures.
Look for model numbers and UPCs listed in the recall notice to confirm if your kit is affected.
Reach out to Medline directly for assistance with the recall process.
The recall states the gel may not meet sterility specifications, so they are not safe for use without replacement.
Check the model numbers and UPCs listed in the recall notice. Products distributed between April 2020 and April 2023 are affected.
Contact Medline directly for instructions on how to return or replace the affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2303-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2303-2023 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.
