Catalog Number 0606600000 |
Device Problems
Disassembly (1168); Material Fragmentation (1261)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/18/2018 |
Event Type
malfunction
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Event Description
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It was reported that prior to the procedure the screw fell out at the end of the device.There was no associated procedure and therefore, no patient involvement or adverse consequences reported.
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Event Description
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It was reported that prior to the procedure the screw fell out at the end of the device.There was no associated procedure and therefore, no patient involvement or adverse consequences 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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Search Alerts/Recalls
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