Catalog Number 3002 EX |
Device Problem
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 01/07/2014 |
Event Type
malfunction
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Event Description
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It was reported via repair work order that the scale was inaccurate due to foot end load cells malfunctioned.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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Supplemental submitted as the investigation concluded that the scale was inaccurate due to foot end load cells malfunctioned.
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Event Description
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It was reported via repair work order that the scale was inaccurate.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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Conclusion - more troubleshooting needed.
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Search Alerts/Recalls
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