Model Number 1365-36-340 |
Device Problems
Device Dislodged or Dislocated (2923); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Joint Dislocation (2374); No Code Available (3191)
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Event Date 07/07/2020 |
Event Type
Injury
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Manufacturer Narrative
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Product complaint # (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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It was reported that the patient femur fractured and dislocated so the doctor replaces head and stem with new revision stem and head.Doi: (b)(6) 2020, dor: (b)(6) 2020, right side.
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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 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.The reported patient code no code available (3191) in the previous medwatch was used to capture device revision or replacement.
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Search Alerts/Recalls
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