Medline recalls custom sterile and non-sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility specifications. Affected kits were distributed 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 standards, which could lead to infections during medical procedures. This recall affects kits distributed between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used during medical procedures. This is a risk for healthcare workers handling the kits in clinical environments.
Healthcare professionals and medical facilities that use these kits for procedures like vein access or ultrasound-guided injections. The risk is primarily for those using the kits in clinical settings where sterility is critical.
Check the model numbers listed in the recall notice (e.g., DYNJ57112, DYNJSPICC2) and UPC numbers provided. These kits were distributed by Medline between April 2020 and April 2023.
Look for the model number on the kit label, such as DYNJ57112 or DYNJSPICC2.
Reach out to Medline Industries for assistance with the recall and to get replacement kits if needed.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Kits with model numbers listed in the recall notice, such as DYNJ57112, DYNJSPICC2, and others, distributed between April 2020 and April 2023.
No, the recall indicates a low-risk issue with sterility standards, so you can continue using the kits but should contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2306-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2306-2023 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.
