Health & Personal Care
HIGH
FDA DEVICE
Omnia Medical TiBrid Fusion Device and Angled Screwdrivers Recalled for Field Instrument Failure (Z-
Omnia Medical issued a recall for 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device and TiBrid SA Angled Screwdrivers after field failures were reported. The recall covers nationwide distribution in AZ, CA, NJ, NV, OK and WA. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Omnia Medical
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