Biomet Microfixation, LLC recalls Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
- Recall date
- April 11, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2073-2017
- FDA classification
- Class II
- Brand / firm
- Biomet Microfixation, LLC
- Sold / distributed
- AL, MO and UT Canada, Australia, Netherlands, and Egypt
Why it was recalled
Part of the number on the tray lid differ from the part number on the base.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
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