Model Number N/A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Bone Fracture(s) (1870); Hip Fracture (2349)
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Event Type
Injury
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Manufacturer Narrative
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(b)(4).Source: (b)(6).Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2020-04255.Concomitant medical devices: unknown stem.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.Device remains implanted in the patient.
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Event Description
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It was reported that during an initial hip arthroplasty, the neck of the femur fractured.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 further event information available at the time of this report.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.D10: catalog number:00811400100; lot number:64521375; brand name: cpt stem.
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Manufacturer Narrative
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The initial was submitted under a wrong manufacturing site.This report should be voided, as it was submitted in error.An updated report will be submitted under the corrected manufacturing site.
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Event Description
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The initial was submitted under a wrong manufacturing site.This report should be voided, as it was submitted in error.An updated report will be submitted under the corrected manufacturing site.
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Search Alerts/Recalls
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