Model Number 3186 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Headache (1880); Depression (2361)
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Event Date 07/19/2019 |
Event Type
Injury
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Manufacturer Narrative
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Date of event is estimated.The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Event Description
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Related manufacturer reference number: 3006705815-2020-01705.It was reported the patient is experiencing headaches and depression.Reprogramming was unable to resolve the issue.Surgical intervention may take place at a later date.
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Event Description
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Additional information received indicates the patient's system was explanted.
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Manufacturer Narrative
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The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Search Alerts/Recalls
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