Device evaluation of the alleged malfunction required retrieval of the device from the patient; return to the contract manufacturer for decontamination, inspection and initial safety and performance testing.Returned therapy cable passed weight, safety, and eit.The returned monitor was tested and passed both isl (safety) and eit (performance) testing.The returned device passed all field return tests and inspections.The reported condition was not able to be replicated.There is no indication of a product malfunction.Will continue to trend for future occurrences.
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