If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Device was used for treatment, not diagnosis.This report is for an unknown device/unknown lot.Part and lot number are unknown; udi number is unknown.(b)(4).
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Asr litigation records received.Litigation alleges pain, swelling, elevated blood cobalt and chromium, injury, discomfort, poor balance, difficulty walking, clicking, bone erosion, femoral and acetabular loosening, impingement, metallosis and emotional distress.Doi: (b)(6) 2009 - dor: (b)(6) 2017 (right hip).
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