Catalog Number 6252000000 |
Device Problems
Difficult or Delayed Positioning (1157); Device Tipped Over (2589)
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Patient Problems
Abrasion (1689); Discomfort (2330)
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Event Date 01/01/2023 |
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 difficult to maneuver the chair which did not result in a tip; device tip.There was 1 event with patient involvement the patient experienced abrasion; discomfort.
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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 was functionally/visually inspected in the field; no defect or malfunction was found.There was no remedial action taken.This device is not labeled for single use.
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Search Alerts/Recalls
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