Catalog Number UNK KNEE TIBIAL INSERT |
Device Problem
Insufficient Information (3190)
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Patient Problems
Pain (1994); Fibrosis (3167); Not Applicable (3189)
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Event Date 03/31/2017 |
Event Type
Injury
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Manufacturer Narrative
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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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Received medical records on (b)(6) 2018.Records reported that patient's right attune total knee was revised to address pain, stiffness, and arthrofibrosis.Revising surgeon performed an extensive synovectomy, lysis of adhesions, and polyethylene insert exchange.Doi: (b)(6) 2015; dor: (b)(6) 2017; (right 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.Depuy synthes considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.If information is obtained that was not available for the initial medwatch , a follow-up medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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