Eden Spine Europe SA GIZA Vertebral Body Replacement recall — FDA Z-2072-2017
Complaints that implants have been disassembled by surgeons because of unscrewing completely the locking screw.
Overview of recall records associated with Eden Spine Europe SA, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Complaints that implants have been disassembled by surgeons because of unscrewing completely the locking screw.
This page summarizes recall records in which the official source identifies Eden Spine Europe SA 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.