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 might not meet sterility standards. This could lead to infections during medical procedures if the kits are used without proper sterilization.
The ultrasound gel component in the kits may not meet sterility specifications, which could lead to contamination if the kits are used in medical procedures without proper sterilization. This poses a risk of infection to patients during procedures.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is low for most users as the kits are designed for sterile environments and the hazard is related to potential contamination.
Check for the model numbers listed in the recall (e.g., DYNJ0842825D, DYNJ49933I) and UPC numbers provided in the recall notice. The kits were distributed between April 2020 and April 2023.
Look for the model numbers and UPCs listed in the recall notice to confirm if your kit is affected.
The ultrasound gel component in the kits may not meet sterility specifications, which could lead to contamination during medical procedures.
Check the model numbers and UPCs listed in the recall notice to confirm if your kit is affected. If it is, you should contact Medline for further instructions.
The risk is low as the kits are designed for sterile environments and the hazard is related to potential contamination if not properly sterilized.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2301-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2301-2023 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.
