The manufacturer received information alleging an issue related to a cpap device's sound abatement foam.Patient alleged having tia, 2 miny strokes, blood clots, high blood pressure and blood is thinning.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
|
The manufacturer previously reported an allegation of an issue related to sound abatement foam. additional information was received and section b5 should be reported as: the manufacturer was contacted in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging an issue related to a continuous positive airway pressure (cpap) device's sound abatement foam.The patient alleged having tia, 2 miny strokes, blood clots, high blood pressure and blood is thinning.There was no medical intervention required by the patient.The reported event of having tia, 2 miny strokes, blood clots, high blood pressure and blood is thinning.And its reported severity was reviewed by the manufacture's clinical expert.This event is assessed as not related to the device in this case.Based on the available information,the manufacture concludes no further action is necessary.There was no medical intervention required by the patient.Repeated attempts to have the device and components returned for evaluation and investigation were unsuccessful.The manufacturer believes they will be unable to gather additional information. the manufacturer is submitting a final report at this time.If pertinent information becomes available to the manufacturer at a later date, an addendum to this final report will be filed. section(s) b1, b2, has changed related to the complaint changing from the reported adverse event to a product problem. section h1 has changed to reflect a malfunction. section h6 health effect- impact code, type of investigation findings and investigation conclusions has been updated.
|
The manufacturer previously submitted mdr 2518422-2022-67346-1 with incorrect sections b1, b2, h1, h6.Corrections to previous mdr are made in this report as follows: section b1 was corrected to adverse event and product problem.(only product problem was checked in previous mdr).Section b2 was corrected to other serious or important medical events.(previously it was blank).Section h1 was changed from malfunction to serious injury.Section h6- health effect - impact code was updated.
|