Medline recalls custom sterile and non-sterile procedural kits containing Turkuaz ultrasound gel due to potential failure to meet sterility specifications. Affected kits were distributed 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 contain Turkuaz ultrasound gel because the gel may not meet sterility standards. This could lead to infections if the kits are used in medical procedures.
The ultrasound gel in these kits may not meet sterility requirements, which could lead to infections if the kits are used in medical procedures. This is a potential contamination risk rather than an immediate hazard.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is primarily for those handling the kits during medical procedures.
Check the model numbers and UPCs listed in the recall notice. The kits were distributed between April 2020 and April 2023 with specific model numbers and corresponding UPCs.
Review the model numbers and UPCs listed in the recall notice to determine if your kit is affected.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used in medical procedures.
Check the model number and UPC on your kit against the list of affected models and UPCs provided in the recall notice.
No, the recall is for potential sterility issues, not an immediate hazard. However, you should check if your kit is affected before use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2300-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2300-2023 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.
