The manufacturer received information in relation to a remstar auto a-flex unit.The patient alleged thathe has a lot of phlegm ,and suspected that this incident is associated with the usage of the device.The device was replaced by a new cpap device on (b)(6) 2023.There was no allegation of serious or permanent harm or injury.No medical intervention was required for the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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