Catalog Number M5722INT0600220 |
Device Problem
Insufficient Information (3190)
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Patient Problem
No Code Available (3191)
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Event Date 11/01/2017 |
Event Type
Injury
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Manufacturer Narrative
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It was reported that the patient had an accident.A revision surgery is planned to exchange the poly insert.Review of the device history record indicates that the device was manufactured to specification.
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Event Description
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It was reported that the patient had an accident.A revision surgery is planned to exchange the poly insert.
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Manufacturer Narrative
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It was originally reported that the patient had an accident.A revision surgery occurred to exchange the poly insert.Following revision surgery, it was reported that the poly insert was dislocated posterolateral.Review of the device history record indicates the device was manufactured to specification.
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Event Description
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It was originally reported that the patient had an accident.A revision surgery occurred to exchange the poly insert.Following revision surgery, it was reported that the poly insert was dislocated posterolateral.
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Search Alerts/Recalls
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