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. Consumers should check model numbers and UPCs listed to determine if their kit is 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. The gel may not meet sterility requirements, which could lead to infections during medical procedures if used improperly.
The ultrasound gel in these kits might not be sterile, which could cause infections if used during medical procedures. This risk is specific to kits used in sterile environments where contamination could lead to health issues.
Healthcare professionals and medical facilities that purchased the recalled kits between April 2020 and April 2023. Those using the kits for procedures where sterility is critical are at higher risk.
Check if your kit has model number DYNJ52283C (UPC 019348965000) or DYNJ61476 (UPC 019348957199). These kits were sold by Medline between April 2020 and April 2023.
Look for model numbers DYNJ52283C or DYNJ61476 on the kit label.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check if your kit has model numbers DYNJ52283C or DYNJ61476. If it does, contact Medline for instructions.
The gel may not be sterile, which could cause infections if used improperly during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2291-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2291-2023 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.
