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Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
Recalled November 18, 2015 · FDA recall Z-0261-2016 · Stryker Howmedica Osteonics
Hazard
Complaints that the femoral head could not be assembled with its corresponding V40 stem trunnion at the time of surgery. · FDA Class II
Units
201
Sold at
Nationwide Distribution
Description
Complaints that the femoral head could not be assembled with its corresponding V40 stem trunnion at the time of surgery.
Product
Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →