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Stryker Howmedica Osteonics Corp. recalls VariAx Compression Plating System
Recalled April 27, 2016 · FDA recall Z-1507-2016 · Stryker Howmedica Osteonics
Hazard
Stryker received two reports indicating that during screw insertion under a high lateral angle a bone screw went through a oblong hole. · FDA Class II
Units
118 units
Sold at
Nationwide Distribution
Description
Stryker received two reports indicating that during screw insertion under a high lateral angle a bone screw went through a oblong hole.
Product
VariAx Compression Plating System
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →