Model Number N/A |
Device Problem
Difficult to Insert (1316)
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Patient Problem
Hip Fracture (2349)
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Event Type
Injury
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Manufacturer Narrative
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(b)(4).Occurred in (b)(6).Once the investigation has been completed, a follow-up mdr will be submitted.
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Event Description
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It was reported that during a hip arthroplasty revision, an intraoperative bone fracture occurred.No additional patient consequences were reported.Attempts have been made and no further information has been provided.
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Event Description
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No further event information available at the time of this report.
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Manufacturer Narrative
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This report is not for a device malfunction.Reported event was unable to be confirmed due to limited information received from the customer.Device history record (dhr) review was unable to be performed as the lot number of the device involved in the event is unknown.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not provided.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Search Alerts/Recalls
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