Home / Recalls / Medical Devices
Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM surgery.
Recalled January 1, 2014 · FDA recall Z-0582-2014 · 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
1,690 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 Rim Impactor Tip Product Usage: Used for MDM surgery.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →