Medical DeviceSep 17, 2025
Omnia Medical TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled recall — FDA Z-2557-2025
Failure of fusion system instruments in the field.
Class IIFDA: OngoingOmnia Medical
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Omnia 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.