Model Number N/A |
Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problem
Joint Dislocation (2374)
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Event Date 11/29/2022 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Product will not be returning for the investigation as the product location is unknown.The investigation is in process.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: 0001825034 - 2022 - 02835.
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Event Description
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It was reported that patient underwent a left hip revision after an unknown amount of time post implantation due to dislocation.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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No additional event details to report at this time.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional and/or corrected information.H6: component code: mechanical (g04) - head.No product was returned, or pictures provided; visual and dimensional evaluations could not be performed.Part and lot identification are necessary for review of device history records, neither were provided.Complaint history review cannot be performed without product identification.Medical records were not provided.A definitive root cause cannot be determined.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Search Alerts/Recalls
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