Catalog Number 102454407 |
Device Problem
Insufficient Information (3190)
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Patient Problem
Pain (1994)
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Event Date 10/30/2017 |
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 pain.
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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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Manufacturer Narrative
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This product was reported in error.No patient death, serious injury or evidence of reportable product malfunction occurred.Depuy considers the investigation closed at this time.Should any additional information be received to change the outcome of the performed investigation, the complaint will be re-opened.
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Manufacturer Narrative
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Product complaint # = > pc-000058307.
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Event Description
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Additional information received indicating that reason for revision was due to arthritis extension.No components were loose.No other significant patient factors were implicated.
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Search Alerts/Recalls
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