Catalog Number 0830000000 |
Device Problem
Device Slipped (1584)
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Patient Problem
No Patient Involvement (2645)
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Event Date 01/01/2020 |
Event Type
malfunction
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Manufacturer Narrative
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This mdr is part of the fda voluntary malfunction summary reporting program.3 devices were evaluated in the field but the issue was not confirmed; no defect or malfunction was found.1 device was evaluated in the field and the issue was confirmed; the device had a broken/damaged component.The devices were repaired and returned.There was no remedial action taken.This device is not labeled for single use.
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Event Description
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This report summarizes 4 malfunction events, where it was reported that the seat was slippery or the seat drifted.There was no patient involvement.
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Search Alerts/Recalls
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