Medline recalls custom sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were sold from April 2020 to April 2023. Contact Medline for details.
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 might not meet sterility standards, which could lead to infections during medical procedures.
The ultrasound gel in the kits may not meet sterility requirements. This could allow bacteria to grow, increasing infection risk during medical procedures.
Healthcare providers using these kits for dialysis or other procedures are most at risk. Patients receiving treatments with these kits could be exposed to non-sterile gel.
Check for model numbers MNS10750A (UPC 10653160356073) or CVI3845 (UPC 10653160270072). These kits were sold by Medline between April 2020 and April 2023.
Look for model numbers MNS10750A or CVI3845 on the kit packaging.
Reach out to Medline for specific instructions on how to return or replace the kit.
The ultrasound gel in these kits may not meet sterility standards, which could lead to infections during medical procedures.
Check the model number on the kit and contact Medline for instructions on returning or replacing it.
The gel might not be sterile, so there is a risk of infection during medical procedures. However, the recall is for low-risk situations.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2313-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2313-2023 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.
