Medline recalls custom sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility standards. Products sold between April 2020 and April 2023 with specific model numbers and UPCs are affected.
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.
The ultrasound gel in the kits may not meet sterility standards. This could allow bacteria to contaminate the gel, increasing the risk of infection during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. Patients undergoing procedures with these kits could face infection risks.
Check for kits labeled 'CATH LAB BASIN PACK' (model DYNJ69864A), 'DELNOR VASCULAR BASIN PACK' (model DYNJ82257), or 'FLAP PACK' (model DYNJ60224C). Products were sold between April 2020 and April 2023 with specific UPC numbers.
Look for the model numbers DYNJ69864A, DYNJ82257, or DYNJ60224C on the kit packaging.
Reach out to Medline customer service for assistance with the recall and to confirm if your product is affected.
The ultrasound gel may not meet sterility standards, which could lead to infections during medical procedures.
Kits labeled 'CATH LAB BASIN PACK' (model DYNJ69864A), 'DELNOR VASCULAR BASIN PACK' (model DYNJ82257), or 'FLAP PACK' (model DYNJ60224C) sold between April 2020 and April 2023.
Check the model number on the kit packaging. Affected kits have model numbers DYNJ69864A, DYNJ82257, or DYNJ60224C and were sold 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-2318-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2318-2023 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.
