The customer contact reported the device alarmed with an e630 (screw rotation error) error code.The device was returned to the biomedical department with a note that stated, "malfunction".No tracking info was provided; therefore, specific patient info, 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 alarmed with an e630 (screw rotation error) error code.No add'l info was provided.
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