Model Number S7 |
Device Problems
Unintended Arm Motion (1033); Unintended Movement (3026)
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Patient Problem
No Patient Involvement (2645)
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Event Date 03/15/2017 |
Event Type
malfunction
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Manufacturer Narrative
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No patient information provided as no patient was involved in this concern.Return requested 03/15/2017.No parts have been received by manufacturer for analysis.
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Event Description
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A medtronic representative reported a site navigation system articulating arm that would not tighten properly.No further details regarding the damage, or how it occurred, were provided.There was no patient present when this issue was identified.
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Manufacturer Narrative
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The suspect vertek arm was received by the manufacturer for evaluation.Testing found that the starburst arm would not completely locked down and when the handle was tightened, the handle was loose and would not release.The hardware investigation found that the reported event was related to a hardware issue.This issue was documented in a medtronic navigation hardware anomaly tracking database.
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Search Alerts/Recalls
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