Omnia Medical Recalls

2 recalls found for Omnia Medical. Check if any of your products are affected.

HIGHFDA DEVICE

Omnia Medical Recalls Intervertebral Fusion Device Over Safety Hazard

Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall follows reports of failure of fusion system instruments in the field. Healthcare providers and patients must stop using the device immediately.

Omnia Medical
Failure of
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HIGHFDA DEVICE

Omnia Medical Recalls Intervertebral Fusion Devices Over Hazard

Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall affects devices distributed nationwide across six states due to potential failure of fusion system instruments. Patients and healthcare providers must stop using the devices immediately to avoid high-risk complications.

Omnia Medical
Failure of
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Brand Statistics

Total Recalls
2
Pages
1