Uoc Usa United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 recall — FDA Z-0110-2022
Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.
Overview of recall records associated with Uoc Usa Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.
This page summarizes recall records in which the official source identifies Uoc Usa 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.