Catalog Number 6001-088-327 |
Device Problem
Image Display Error/Artifact (1304)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 12/20/2018 |
Event Type
malfunction
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Event Description
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It was reported that during set up for a procedure at the user facility, the device was found to be bent.The procedure was completed successfully without a clinically significant delay; no adverse consequences or medical intervention were reported.
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Manufacturer Narrative
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Device evaluation: follow-up report submitted to document device evaluation results.
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Event Description
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It was reported that during set up for a procedure at the user facility, the device was found to be bent.The procedure was completed successfully without a clinically significant delay; no adverse consequences or medical intervention were reported.
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Search Alerts/Recalls
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