H3: evaluation determined the device was overheating, and the maximum temperature was measured to be 137°f.The likely cause of failure was identified as motor was worn.It was also noted that the cable had been damaged.Date of notification: 2024-jan-31 medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
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