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. Contact Medline for details.
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.
The ultrasound gel in these kits may not meet sterility standards, potentially leading to infections during medical procedures. This is a risk for procedures involving sterile environments like surgeries or diagnostic imaging.
Healthcare professionals and medical facilities that purchased these kits between April 2020 and April 2023 are likely affected. Patients undergoing procedures using these kits may be at risk of infection.
Check for kits labeled as CAROTID, CENTRAL LINE INSERTION, or other specific models listed with model numbers starting with DYNJ or CDS. These kits were sold by Medline between April 2020 and April 2023.
Look for model numbers such as DYNJ54287A or CDS983069G on the kit packaging.
Reach out to Medline Industries for assistance with returning or replacing the affected kits.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Kits labeled as CAROTID, CENTRAL LINE INSERTION, or other specific models with model numbers listed in the recall (e.g., DYNJ54287A, CDS983069G) sold between April 2020 and April 2023.
Check the model number on the kit packaging against the list of affected models provided in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2309-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2309-2023 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.
