FDAMay 18, 2015device

ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw, Standard Implant Grade Titanium Alloy Rx Only Provided Non-Sterile Do Not Reuse

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The Firebird Spinal Fixation System 6.5 mm x 55 mm Bone Screw, Self-Tapping is currently mislabeled at the distal tip of the bone screw showing a length measurement of 50 mm instead of 55 mm.

What to do

FDA enforcement status: Terminated

Brands named

orthofix

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw, Standard Implant Grade Titanium Alloy Rx Only Provided Non-Sterile Do Not Reuse — Recall Details · AllClear