Catalog Number 5700000000 |
Device Problem
Device Operates Differently Than Expected (2913)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 10/11/2017 |
Event Type
malfunction
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Manufacturer Narrative
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Distributor performed evaluation and any necessary correction.
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Event Description
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It was reported by the distributor that the brakes were not set correctly, potentially resulting in reduced brake force.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 brakes were not set correctly, potentially resulting in reduced brake force.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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