United Orthopedic USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray recall — FDA Z-1217-2024
Their is a potential that the implant curved stem may be oriented incorrectly.
Overview of recall records associated with United Orthopedic Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 3.
Their is a potential that the implant curved stem may be oriented incorrectly.
Their is a potential that the implant curved stem may be oriented incorrectly.
Their is a potential that the implant curved stem may be oriented incorrectly.
This page summarizes recall records in which the official source identifies United Orthopedic Corporation 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.