Model Number 3228 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Therapeutic Effects, Unexpected (2099)
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Event Type
Injury
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Manufacturer Narrative
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The manufacturer 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.The manufacturer defers to the patient's physician regarding medical history.
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Event Description
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It was reported the patient was experiencing pain in the rib area whether the scs system stimulation was on or off.Subsequently, the patient's scs lead was revised and moved more midline.No further information was available at this time.
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Event Description
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Follow up information received identified the patient reported the rib pain was gone.The patient stated she believed the issue was not due to the stimulator at all.
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Search Alerts/Recalls
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