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.
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 these kits might not meet sterility requirements, meaning it could be contaminated. This contamination could lead to infections during medical procedures if the gel is not properly sterile.
Healthcare providers using these kits for procedures like fetoscopy or breast biopsies are most at risk. Patients undergoing procedures with these kits could face infection if the gel is not sterile.
Check for model numbers DYNJ906905B, CDS840215O, DYNJ906905A, or DYNDH1187A on the kit packaging. These kits were sold by Medline between April 2020 and April 2023 with specific UPC numbers.
Look for model numbers DYNJ906905B, CDS840215O, DYNJ906905A, or DYNDH1187A on the kit packaging.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check the model number and UPC on the packaging. If it matches the listed models, contact Medline for further instructions.
The gel may not be sterile, which could lead to infections during medical procedures. However, the recall is for low-risk scenarios.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2310-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2310-2023 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.
