Medline recalls breast biopsy procedural kits with Turkuaz ultrasound gel that may not meet sterility specifications. 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 breast biopsy 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 sold between April 2020 and April 2023.
The ultrasound gel in these kits may not meet sterility specifications, potentially leading to infections if used in medical procedures. This risk arises because the gel is part of sterile procedural kits intended for clinical use.
Healthcare professionals and patients using breast biopsy kits with Turkuaz ultrasound gel. Those most at risk are individuals undergoing procedures requiring sterile equipment.
Check for model numbers: DYNDA1224A, DYNDA1224B, SPEC0130C, MNS11895, DYNDH1496, DYNDH1319, or DYNDH1187A. These kits were sold by Medline between April 2020 and April 2023 with specific UPC numbers listed in the recall.
Look for model numbers on the kit: DYNDA1224A, DYNDA1224B, SPEC0130C, MNS11895, DYNDH1496, DYNDH1319, or DYNDH1187A.
Confirm the kit matches the listed UPC numbers for the specific model to ensure it is affected.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
These kits were sold by Medline between April 2020 and April 2023.
Check the model number on your kit against the list: DYNDA1224A, DYNDA1224B, SPEC0130C, MNS11895, DYNDH1496, DYNDH1319, or DYNDH1187A. Also verify the UPC numbers provided in the recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2339-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2339-2023 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.
