Additional information was received that the reported suction failure was not confirmed.According to the service record, the equipment was checked and found to function within manufacturing specifications.The reported complaint could not be duplicated.The reported complaint will be noted during preuse testing, as contained in the user manual.Standard of care includes ensuring adequate backup equipment.The reported complaint will not affect delivery of o2, agent or ventilation from the anesthesia machine.The initial mdr was not reportable.
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