Catalog Number 150600006 |
Device Problem
Malposition of Device (2616)
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Patient Problem
Pain (1994)
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Event Date 12/06/2017 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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The patient was revised to address painful left total knee.Components were not loose and the tibia had excessive slope per the surgeon.Doi:unknown; dor: (b)(6) 2017; left knee.
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Manufacturer Narrative
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(b)(4).Investigation summary = > no device associated with this report was received for examination.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. .
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Search Alerts/Recalls
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