Model Number N/A |
Device Problems
Malposition of Device (2616); Insufficient Information (3190)
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Patient Problem
No Information (3190)
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Event Date 01/08/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Date of birth: unknown month and day in 1967.Report source: foreign: (b)(6).The device will not be returned for analysis, due to location of device is unknown; however, an investigation of the reported event is in progress.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2020-00350, 0001822565-2020-00356, 0001822565-2020-00357.
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Event Description
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It was reported that the patient underwent a revision procedure for an unknown reason.Attempts have been made and additional information on the reported event is unavailable at this time.
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Event Description
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It was reported that the patient underwent a revision procedure to fix the angulation of the shell.Attempts have been made and additional information on the reported event is unavailable at this time.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.
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Manufacturer Narrative
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Upon reassessment of the reported event, the head was determined to be not reportable.The initial report was forwarded in error and should be voided.
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Event Description
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Upon reassessment of the reported event, the head was determined to be not reportable.The initial report was forwarded in error and should be voided.
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Search Alerts/Recalls
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