Catalog Number 5407120950A |
Device Problems
Leak/Splash (1354); Overheating of Device (1437)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 05/12/2016 |
Event Type
malfunction
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Event Description
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It was reported that during a surgical procedure at the user facility the device was overheating, and was leaking an unknown substance.The procedure was completed successfully.No clinically significant delay, no medical intervention and no adverse consequences were reported with this event.
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Manufacturer Narrative
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Follow-up report submitted to document device evaluation results.
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Event Description
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It was reported that during a surgical procedure at the user facility the device was overheating, and was leaking an unknown substance.The procedure was completed successfully.No clinically significant delay, no medical intervention and no adverse consequences were reported with this event.
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Search Alerts/Recalls
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