MEDTRONIC NEUROMODULATION NURO; STIMULATOR,PERIPHERAL NERVE,NON-IMPLANTED,FOR PELVIC FLOOR DYSFUNCTION
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Model Number 3533 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Complaint, Ill-Defined (2331)
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Event Type
Injury
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Manufacturer Narrative
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A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Event Description
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The patient reported that they had to have surgery.The patient also reported that they had machines on them to ¿pull the poisoned blood out.¿ it was noted that the patient did not know how long they were going to be in this predicament but they were helping them a lot.The patient stated that they were feeling so much better than before.It was unknown if any environmental/external/patient factors that may have led or contributed to the issue.The patient had completed 12 ptnm sessions and was alive with no injury.No further complications are anticipated.
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Search Alerts/Recalls
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