Advance Medical Designs recalls procedural kits containing ultrasonic transmission gel with mislabeled use instructions. Affected items include specific item numbers and lot numbers. Consumers should check their kits for the listed identifiers.
Ultrasound gel mislabeled with inappropriate use.
Advance Medical Designs is recalling procedural kits that contain ultrasonic transmission gel with mislabeled use instructions. This could lead to improper use of the gel, potentially causing harm during medical procedures.
The ultrasonic transmission gel is mislabeled with inappropriate use instructions. This could result in improper application during medical procedures, potentially causing ineffective imaging or other issues.
Medical professionals and individuals using these procedural kits for ultrasound imaging. Those who have the specific item numbers and lot numbers listed are most at risk.
Check your procedural kits for item numbers starting with 28-GG (e.g., 28-GG023, 28-GG105) and corresponding lot numbers listed in the recall notice. The gel is part of ultrasound imaging kits.
Look for item numbers such as 28-GG023, 28-GG105, or other listed codes on the gel packaging.
Check the lot numbers provided in the recall notice for affected items, such as 20794C0208 for item 28-GG023.
The ultrasonic transmission gel is mislabeled with inappropriate use instructions, which could lead to improper application during medical procedures.
Check your procedural kits for item numbers like 28-GG023, 28-GG105, or other listed codes, and verify the corresponding lot numbers from the recall notice.
No, the recall indicates a mislabeling issue, not an immediate safety hazard. However, you should check your kits for the listed item and lot numbers.
We’ve drafted a message you can send Advance Medical Designs to request your refund or repair — edit it as you like.
Subject: Recall Z-2537-2023 — Advance Medical Designs Advance Medical Designs Hello, I own a Advance Medical Designs that is covered by recall Z-2537-2023 from Advance Medical Designs. 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.
