Medline recalls custom sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were sold between April 2020 and April 2023 with specific model numbers and UPCs listed.
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 include 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 requirements. This could allow bacteria to grow, increasing the risk of infections during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving procedures with these kits could face infection risks.
Check for the model numbers listed in the recall notice (e.g., DYNDA2482, ART920) and UPC numbers distributed between April 2020 and April 2023.
Identify the model number on the kit to see if it matches the list of affected models provided in the recall.
Reach out to Medline directly for assistance with the recall process or to confirm if your kit is affected.
The recall applies to specific kits used in medical procedures. If your kit matches the listed models, there is a risk of non-sterile gel that could lead to infections.
Check the model number on your kit against the list of affected models and UPC numbers provided in the recall notice. Kits distributed between April 2020 and April 2023 are included.
Contact Medline directly to confirm if your kit is affected and to get instructions on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2323-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2323-2023 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.
