Medline recalls custom 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 procedural kits that contain Turkuaz ultrasound gel because the gel might not be sterile. This could lead to infections during medical procedures if the gel is used without proper sterility.
The ultrasound gel in the kits may not meet sterility standards, which means it could be contaminated. If used during medical procedures, this contamination could lead to infections in patients or healthcare workers.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving procedures with non-sterile gel could face infection.
Check for kits labeled 'PROBE COVER PACK' with model number DYNDA1219. These were sold by Medline between April 2020 and April 2023 with UPC 10888277283879.
Look for the model number DYNDA1219 on the kit label to confirm if it's affected.
The recall states the gel may not meet sterility specifications, which could lead to infections during medical procedures. However, the hazard level is low risk as the remedy does not require immediate stop-use.
Check for kits labeled 'PROBE COVER PACK' with model number DYNDA1219 sold by Medline between April 2020 and April 2023.
The recall does not specify a remedy, so contact Medline directly 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-2329-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2329-2023 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.
