The customer contact reported the device alarmed with an e630 (screw rotation error) error code.The device was returned to the biomedical department with an unsigned note that stated, "pca is stopping on its own and alarm wasn't stop".No tracking info was provided; therefore, specific pt info, pump programming, or event details were not available.There were no reports of any adverse events or delays in critical therapies while the device was in clinical use.During testing at the user facility, an e630 (screw rotation error) error code was noted.Though requested, no add'l info was provided.
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