Catalog Number 5700000000 |
Device Problem
Bent (1059)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 07/13/2017 |
Event Type
malfunction
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Manufacturer Narrative
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Distributor performed evaluation and any necessary repair.Distributor performed evaluation and any necessary repair.
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Event Description
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It was reported by the distributor that the power cord prongs were bent.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Event Description
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It was reported by the distributor that the power cord prongs were bent.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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