Model Number N/A |
Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problems
Joint Dislocation (2374); Patient Problem/Medical Problem (2688)
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Event Date 01/13/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Concomitant medical products: 110024465 ¿ g7 dual mobility liner ¿ 919620; 010000706 ¿ g7 shell ¿ 6455977; 00811400410 ¿ femoral stem ¿ 63051144; 00877502803 ¿ biolox delta head ¿ 2947385.Report source: (b)(6).Customer has indicated that the product will not be returned to zimmer biomet 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: 0001825034-2020-00529.
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Event Description
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It was reported that patient underwent a right hip revision approximately 10 months 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 information to report at this time.
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Manufacturer Narrative
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Reported event was unable to be confirmed due to limited information provided by the customer.Dhr was reviewed and no discrepancies were found.The root cause is unable to be determined.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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