Model Number MN20450-90A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Numbness (2415)
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Event Date 10/07/2020 |
Event Type
Injury
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Manufacturer Narrative
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The results/method and conclusion codes along with investigation results will be provided in the final report.
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Event Description
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Related manufacturer reference number: 1627487-2020-33102.Related manufacturer reference number: 1627487-2020-33103.It was reported that the patient was experiencing post-op surgical pain and light numbness in the upper thigh.The patient was hospitalized and ct scans showed no adverse findings.As a result, the physician removed the patient's leads.
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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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