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Omnia Medical recalls TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60
Recalled September 17, 2025 · FDA recall Z-2557-2025 · Omnia Medical
Hazard
Failure of fusion system instruments in the field. · FDA Class II
Units
15 units
Sold at
US Nationwide distribution in the states of AZ, CA, NJ, NV, OK & WA.
Description
Failure of fusion system instruments in the field.
Product
TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60 degree angles.
Manufacturer(s)
Omnia Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →