Catalog Number 0190000000 |
Device Problems
Break (1069); 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 04/17/2018 |
Event Type
malfunction
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Event Description
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It was reported that the siderail is broken and will not latch upright.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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The device could not be located at the customer facility.
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Event Description
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It was reported that the siderail is broken and will not latch upright.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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