XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use recall — FDA Z-0429-2021
Cervical Implants contain a label that incorrectly identifies the grade of titanium used.
Overview of recall records associated with XTANT Medical, including dates, categories and classifications where available.
Classification mix: Class III: 1.
Cervical Implants contain a label that incorrectly identifies the grade of titanium used.
This page summarizes recall records in which the official source identifies XTANT Medical 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.