Class II

Medical Device Recall: TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60 degree angles.

Omnia Medical · July 15, 2024

Reason for Recall

Failure of fusion system instruments in the field.

Distribution

US Nationwide distribution in the states of AZ, CA, NJ, NV, OK & WA.

States Affected

NATIONWIDE

Quantity Affected

15 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2557-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Omnia Medical Medical Device Recall: TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60 degree angles. | SafeCheck