Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
- Recall date
- September 8, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0261-2016
- FDA classification
- Class II
- Brand / firm
- Stryker Howmedica Osteonics Corp.
- Sold / distributed
- Nationwide Distribution
Why it was recalled
Complaints that the femoral head could not be assembled with its corresponding V40 stem trunnion at the time of surgery.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
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