Model Number 24970A |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 07/11/2017 |
Event Type
malfunction
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Manufacturer Narrative
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Without a device serial number, the manufacturing date cannot be determined.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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It was reported during lead analysis testing of the atrial channel, the following message was displayed and the screen froze - "unexpected error occurred.Close the application and contact a medtronic representative." the case was finished with a legacy programmer/analyzer.No patient complications have been reported as a result of this event.The mobile programmer application remains in use.
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Manufacturer Narrative
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Further review prompted a change in the device analysis results.If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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