Catalog Number 6003-200-010 |
Device Problem
Disassembly (1168)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/13/2016 |
Event Type
malfunction
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Event Description
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It was reported that during incoming inspection at the manufacturer facility the device was disassembled.No patient involvement or procedural delays were reported with this event.
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Manufacturer Narrative
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During the visual inspection it was not observed that the device was broken off in parts.
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Event Description
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It was reported that during incoming inspection at the manufacturer facility the device was disassembled.No patient involvement or procedural delays were reported with this event.
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Search Alerts/Recalls
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