Medline recalls custom sterile and non-sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility specifications. Affected kits were sold between April 2020 and April 2023. Check model numbers and UPCs listed for affected items.
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. Affected kits were sold between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, meaning it could be contaminated. This poses a risk of infection during medical procedures if the gel is used without proper sterility.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023 are likely affected. The risk is low as the issue relates to potential sterility failures rather than immediate harm.
Check the model numbers and UPCs listed in the recall notice. Affected kits were sold between April 2020 and April 2023. The kits are labeled with specific model names like 'CHN OR', 'CUSTOM GYN', etc.
Look for the model numbers listed in the recall notice, such as DYNJ902540N or DYNJ63257B, to confirm if your kit is affected.
Reach out to Medline directly to confirm if your specific kit is affected and to get instructions for returning or replacing it.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check the model numbers and UPCs listed in the recall notice. Affected kits were sold between April 2020 and April 2023.
No, the recall is for potential sterility issues, not an immediate safety hazard. Contact Medline to confirm if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2333-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2333-2023 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.
