Catalog Number 2141000000 |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/09/2014 |
Event Type
malfunction
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Event Description
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It was reported that the bed was showing a base tilt error.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 that the bed was showing a base tilt error due to a faulty wiring harness.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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It was initially reported that the bed was showing a base tilt error.Follow-up submitted as further investigation determined the base tilt error was due to a faulty wiring harness.Conclusion code was also updated.
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Manufacturer Narrative
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Conclusion-parts on order.
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Search Alerts/Recalls
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