Medline recalls pediatric procedural kits with Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were sold from April 2020 to April 2023. Consumers should check model numbers and lot dates.
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Medline is recalling pediatric procedural kits that contain Turkuaz ultrasound gel because the gel might not be sterile. This could lead to infections if used on children during medical procedures. Affected kits were sold between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility standards, which could lead to infections if used on children during medical procedures. This risk is specific to kits labeled as pediatric and sold during the recall period.
Parents and healthcare providers using pediatric procedural kits with Turkuaz ultrasound gel. Children receiving medical procedures are at the highest risk of infection.
Check for model number DYNJ45158A on the kit. The kits were sold with UPC 088827750721 and distributed from April 1, 2020, to April 28, 2023.
Look for model number DYNJ45158A on the kit label.
Reach out to Medline for assistance with the recall.
The ultrasound gel may not meet sterility standards, so they are not safe for use on children without proper testing.
Check for model number DYNJ45158A and UPC 088827750721, sold between April 1, 2020, and April 28, 2023.
Contact Medline for assistance with the recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2294-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2294-2023 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.
