Medline recalls custom sterile procedural kits containing Turkuaz ultrasound gel that may not meet sterility standards. Affected kits were sold from April 2020 to April 2023 with specific model numbers.
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 may 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 enter the body during medical procedures, potentially causing infections.
Healthcare providers using these kits for medical procedures are most at risk. Patients undergoing procedures with these kits could face infection risks.
Check for kits labeled 'DR MOTT DRAPE PACK' with model number DYNJ42065B. These were sold between April 2020 and April 2023 with UPC 088827789355.
Look for the model number DYNJ42065B on the kit label.
The ultrasound gel may not meet sterility specifications, which could lead to infections during medical procedures.
Check the kit label for model number DYNJ42065B. If it matches, contact Medline for guidance.
These kits were distributed from Medline between April 2020 and April 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2328-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2328-2023 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.
