Catalog Number 163661 |
Device Problem
Detachment of Device or Device Component (2907)
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Patient Problem
No Code Available (3191)
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Event Date 12/24/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Customer has indicated that the product will not be returned to zimmer biomet for investigation as the product has been retained by patient.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.(b)(4).Multiple mdr reports were filed for this event, please see associated reports: (b)(4).
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Event Description
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It was reported that during patient was revised approximately 3 weeks post implantation due to disassociation.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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Upon reassessment of the reported event, it was determined to be not reportable.The initial report was forwarded in error and should be voided.
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Manufacturer Narrative
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Upon reassessment of the reported event, it 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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