The defect caused the patient to have a delay in the intubation procedure.There was no patient injury, this incident will be reported.Intubation was hindered which delays in establishing a protected airway.Which increases the risk to the patient.Based on the reported information and the event originating in the us, the criteria for reporting an adverse event have been met.
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The defect caused the patient to have a delay in the intubation procedure.There was no patient injury, this incident will be reported.Intubation was hindered which delays in establishing a protected airway.Which increases the risk to the patient.Based on the reported information and the event originating in the us, the criteria for reporting an adverse event have been met.This complaint could not be confirmed because product or pictures were not returned.When a sample from the same lot was tested, the device functioned as intended.The light failure could be re-created if the lamp was partially unscrewed and the handle was re-assembled.It is possible that the customer did not fully screw in the lamp post-cleaning or the lamp had fully burnt out and needed to be replaced.According to ra-46, r33 or reduced visualization due to incorrect battery placement, the risk severity is 5 = significant and does not need to be reviewed at carb.
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