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Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Surgery.
Recalled January 1, 2014 · FDA recall Z-0583-2014 · Stryker Howmedica Osteonics
Hazard
Stryker has received complaints associated with cracks and/or fracture of the Ball Impactor Tip and Rim Impactor Tip Instruments. · FDA Class II
Units
1,024 units
Sold at
USA Nationwide Distribution
Description
Stryker has received complaints associated with cracks and/or fracture of the Ball Impactor Tip and Rim Impactor Tip Instruments.
Product
Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Surgery.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →