FDAApril 7, 2020device

Oryx Cervical Screw Caddy, Model Number BTA-172, as part of the Oryx Cervical Plate System - Product Usage: The Cervical Plate System is intended for use in anterior cervical fixation.

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

The hazard

Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and Variable rescue screws. The caddy location labeled as "Fixed" should be labeled as "Variable" and the caddy location labeled as "Variable" should be labeled as "Fixed. If user installs a fixed rescue screw instead of variable, the screw head may not be flush, it could back out, which could interfere with the cover screw.

What to do

FDA enforcement status: Terminated

Brands named

innovasis

Recall history

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

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