Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel due to potential failure to meet sterility specifications. Kits sold between April 2020 and April 2023 with specific model numbers and UPCs are affected.
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 because the gel might not meet sterility standards. This could lead to infections if the kits are used in medical procedures.
The ultrasound gel in these kits may not meet sterility standards, which could lead to infections during medical procedures. This risk is specific to the gel component within the kits, not the entire kit.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023 are likely affected. Patients using these kits for procedures may be at risk of infection if the gel is not sterile.
Check for kits labeled with model numbers listed in the recall (e.g., DYNJ908249A, ECVC7410A) sold between April 2020 and April 2023. Each kit has a specific model number and UPC code that matches the recall list.
Look for the model number and UPC code on the kit to confirm if it matches the list of affected items in the recall.
Reach out to Medline Industries for assistance with returning or replacing the affected kits.
The recall is due to potential failure of the Turkuaz ultrasound gel to meet sterility specifications, which could lead to infections during medical procedures.
Check the model number and UPC code on your kit against the list of affected items provided in the recall notice, which includes specific model numbers and UPCs sold between April 2020 and April 2023.
No, the recall does not require immediate discontinuation. However, affected kits should be checked and returned or replaced as per Medline's instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2297-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2297-2023 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.
