BOSTON SCIENTIFIC NEUROMODULATION VERTIFLEX INSTRUMENT PLATFORM; PROSTHESIS, SPINOUS PROCESS SPACER/PLATE
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Model Number 140-9800 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Complaint, Ill-Defined (2331); Insufficient Information (4580)
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Event Date 12/15/2020 |
Event Type
Injury
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Event Description
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It was reported that during a spacer implant procedure, after the anesthesia was administered and the incision was made, yet prior to implanting the device, the patient experienced cardiac issues.The procedure was aborted and the patient was doing well after the event.The event was not device related as the device was not used.The device was disposed of by the medical facility.
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Event Description
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It was reported that during a spacer implant procedure, after the anesthesia was administered and the incision was made, yet prior to implanting the device, the patient experienced cardiac issues.The procedure was aborted and the patient was doing well after the event.The event was not device related as the device was not used.The device was disposed of by the medical facility.
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