The customer contact reported the device did not alarm when a distal occlusion was present.The device was returned to the biomedical department for an unspecified reason.No tracking information was provided; therefore, specific patient information, pump programming, or event details were not available.There were no reports of any adverse patient events or delays in critical therapies while the device was in clinical use.During testing at the user facility, the device did not alarm when a distal occlusion was present.Though requested, no additional information was provided.
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