FDAJune 25, 2019device

MAGEC 1 System

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

The hazard

Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.

What to do

FDA enforcement status: Ongoing

Brands named

nuvasive specialized orthopedicsnuvasivenuvasive specialized

Recall history

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

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