Catalog Number 0000000001 |
Device Problem
Bent (1059)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 06/06/2017 |
Event Type
malfunction
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Event Description
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It was reported that the power cord was difficult to connect due to bent prongs.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Manufacturer Narrative
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Date of manufacture added.
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Event Description
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It was reported that the power cord was difficult to connect due to bent prongs.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Search Alerts/Recalls
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