This medwatch report was identified as a late submission during a two year retrospective review of complaints and mdr¿s following receipt of an untitled letter issued by the fda.The carefusion fse went onsite and found that the airway line which is connected to the transducer had mucus.Replaced the xdcr and the airway tube assembly and performed necessary calibrations and ventilator performance checks.The unit is working as per manufactures specification.As of this date the xdcr has not been received for evaluation.When it has been received and evaluated a supplement will be filed.
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