Advance Medical Designs Procedural kits containing ultrasonic transmission gel, Item recall — FDA Z-2536-2023
Ultrasound gel mislabeled with inappropriate use.
Overview of recall records associated with Advance Medical Designs, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Ultrasound gel mislabeled with inappropriate use.
Ultrasound gel mislabeled with inappropriate use.
This page summarizes recall records in which the official source identifies Advance Medical Designs, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.