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Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp.
Recalled February 19, 2014 · FDA recall Z-0964-2014 · Stryker Howmedica Osteonics
Hazard
Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle. · FDA Class II
Units
211 units
Sold at
IL MA, MN, ND, OR, & PA
Description
Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle.
Product
Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France Made in USA non-sterile
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →