Model Number 3228 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Cramp(s) (2193)
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Event Date 07/19/2017 |
Event Type
Injury
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Manufacturer Narrative
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Abbott has limited information related to the patient¿s medical history and is unable to form an opinion as to the relevancy of the patient¿s history to the event reported.Abbott defers to the patient¿s physician regarding medical history.
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Event Description
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It was reported the patient experienced painful stimulation with intermittent cramping.Reprogramming was unsuccessful in resolving the issue.As a result, the patient underwent a lead revision where the original lead was replaced with a different model.
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Event Description
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Follow up information identified that the patient's cramping has improved.
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Event Description
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Follow up information identified the patient cramping has resolved.
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Search Alerts/Recalls
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