Medline recalls custom sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility standards. Affected kits sold between April 2020 and April 2023. Consumers should check 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. The gel may not meet sterility requirements, which could lead to infections if used in medical procedures.
The ultrasound gel in the kits might not meet sterility standards, meaning it could be contaminated. If used in medical procedures, this contamination could lead to infections in patients.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023. Those using the kits for procedures where sterility is critical are at higher risk.
Check the model numbers and UPCs listed in the recall notice. The kits were sold by Medline between April 2020 and April 2023. Specific model numbers include DYNJ33638J, DYNJRA1543, and others.
Look for the model numbers listed in the recall notice, such as DYNJ33638J, DYNJRA1543, and others.
Reach out to Medline directly to confirm if your kit is affected and get instructions for replacement or return.
The recall states the gel may not meet sterility standards, so they should not be used until the issue is resolved.
Check the model numbers and UPCs listed in the recall notice. Contact Medline for instructions on replacement or return.
The kits were distributed by Medline between April 2020 and April 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2295-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2295-2023 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.
