Stryker Howmedica Osteonics Corp. recalls VariAx Compression Plating System
- Recall date
- October 10, 2013
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1507-2016
- FDA classification
- Class II
- Brand / firm
- Stryker Howmedica Osteonics Corp.
- Sold / distributed
- Nationwide Distribution
Why it was recalled
Stryker received two reports indicating that during screw insertion under a high lateral angle a bone screw went through a oblong hole.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
VariAx Compression Plating System
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