Catalog Number 5700000000 |
Device Problems
Bent (1059); False Reading From Device Non-Compliance (1228)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 01/22/2017 |
Event Type
malfunction
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Manufacturer Narrative
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The customer was informed that the bed cannot be reapired, and they were advised to scrap the unit.
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Event Description
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It was reported that the scale is inaccurate due to a bent frame.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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