Catalog Number 6007003150 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Bone Fracture(s) (1870)
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Event Date 04/19/2021 |
Event Type
Injury
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Event Description
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On (b)(4) 2021 a total knee procedure was performed at the user facility, on (b)(6) 2021 the patient experienced a supra femoral fracture in the same area.The patient was treated for the fracture.There are no further known adverse consequences or medical intervention associated with the event.
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Manufacturer Narrative
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Device evaluation: follow-up report submitted to document device evaluation results h3 other text: no product return per the customer.
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Event Description
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On (b)(6) 2021 a total knee procedure was performed at the user facility, on (b)(6) 2021 the patient experienced a suprafemoral fracture in the same area.The patient was treated for the fracture.There are no further known adverse consequences or medical intervention associated with the event.
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Search Alerts/Recalls
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