U2 Total Knee System Femoral valgus adaptor, left and right recall — FDA Z-2885-2026
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Overview of recall records associated with United Orthopedic Corp., including dates, categories and classifications where available.
Classification mix: Class II: 6.
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
This page summarizes recall records in which the official source identifies United Orthopedic Corp. 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.