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Instratek, Incorporated recalls Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Scr
Recalled October 1, 2014 · FDA recall Z-2679-2014 · Instratek, Incorporated
Hazard
Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set. · FDA Class II
Units
96
Sold at
Nationwide: Maine, Oregon, Florida, Texas, Virginia, Arizona, Nebraska, California, Ohio, Illinois, Oklahoma, Washington, North Carolina, Arkansas, Tennessee, New Mexico, Connecticut, Colorado
Description
Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set.
Product
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
Manufacturer(s)
Instratek, Incorporated
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →