Genesys spine, Binary Screwdriver, GCP221, component of the Binary Anterior Cervical Plating recall — FDA Z-0040-2018
Unanticipated technique for a cervical screw insertion caused the tip of the threaded inner shaft to break off.
Overview of recall records associated with Genesys Orthopedics Systems, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Unanticipated technique for a cervical screw insertion caused the tip of the threaded inner shaft to break off.
This page summarizes recall records in which the official source identifies Genesys Orthopedics Systems, LLC 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.