Model Number 1217-30-052 |
Device Problem
Malposition of Device (2616)
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Patient Problem
No Code Available (3191)
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Event Date 10/07/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(6).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 due to experiencing hip dislocations.Removed well fixed cup, screw, liner and head.Original implant date unknown.Doi: unknown, dor: (b)(6) 2020, unknown hip.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.
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Search Alerts/Recalls
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