Catalog Number 0408600000 |
Device Problem
Overheating of Device (1437)
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Patient Problem
No Patient Involvement (2645)
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Event Date 10/19/2015 |
Event Type
malfunction
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Event Description
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It was reported that during testing conducted at the user facility the device was overheating.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Manufacturer Narrative
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The device was scrapped following testing.
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Event Description
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It was reported that during testing conducted at the user facility the device was overheating.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Search Alerts/Recalls
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