Model Number N/A |
Device Problem
Insufficient Information (3190)
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Patient Problem
Insufficient Information (4580)
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Event Date 07/22/2021 |
Event Type
Injury
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Event Description
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It was reported the patient underwent an initial right hip arthroplasty.Subsequently, the patient was revised three (3) years post implantation for unknown reasons.
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Manufacturer Narrative
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(b)(4).D10: unknown m/l taper unknown.Multiple mdr reports were filed for this event, please see associated reports: 0001822565 - 2024 - 00673.Customer has indicated that the product will not be returned to zimmer biomet for investigation.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
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Manufacturer Narrative
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Upon receipt of additional information, it was determined this product should not have been reported under this mfr number.This report should be voided, and a corrected report will be filed under (b)(4).
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Event Description
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No additional event information to report at this time.
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Search Alerts/Recalls
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