Catalog Number 300900000000 |
Device Problem
Patient Device Interaction Problem (4001)
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Patient Problem
Fall (1848)
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Event Date 10/01/2023 |
Event Type
malfunction
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Event Description
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This report summarizes 1 malfunction event, where it was reported the device experienced tripping hazard.There was 1 event with patient involvement; no adverse consequences were reported.
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Manufacturer Narrative
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This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device is pending evaluation.There was no remedial action taken.This device is not labeled for single use.
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Manufacturer Narrative
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The device that was pending was evaluated in the field but the issue was not confirmed; no defect or malfunction was found.
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Event Description
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This report summarizes 1 malfunction event, where it was reported the device experienced tripping hazard.There was 1 event with patient involvement; no adverse consequences were reported.
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Search Alerts/Recalls
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