FDAFebruary 13, 2020device

NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provid...

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

The hazard

Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.

What to do

FDA enforcement status: Terminated

Brands named

nuvasive

Recall history

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

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