Model Number MN10450-50A |
Device Problem
Material Fragmentation (1261)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 06/16/2022 |
Event Type
Injury
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Event Description
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It was reported during a lead revision (related manufacturer reference number: 1627487-2022-03486) while removing the l5 lead an incision was made but the lead would not move so the physician decided to cut the lead and leave the remaining portion implanted in the patient.
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Manufacturer Narrative
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During processing of this complaint, attempts were made to obtain complete patient information.Further information was requested but not received.
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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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