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 01/24/2024 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).G2 - foreign: japan.D10: concomitant medical products: medical product - unknown oxford fem; catalog #: unknown; lot #: unknown.Medical product - unknown oxford tib; catalog #: unknown; lot #: unknown.The device will not be returned for analysis; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch 3500a will be submitted.
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Event Description
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It was reported that a patient underwent a uni knee arthroplasty.Subsequently, approximately 5 years later and due to falling and twisting their leg, revision surgery was performed due to bearing dislocation.Attempts have been made and no further information has been provided.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.A review of the device manufacturing records confirmed no abnormalities or deviations.Device is used for treatment.Medical records were not provided.With the available information, a definitive root cause could not 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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Event Description
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No further event information available at the time of this report.
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Search Alerts/Recalls
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