The customer contact reported an e360 (screw rotation error) error code was noted.The device was returned to the biomedical dept for an unspecified reason.No tracking info was provided; therefore, specific pt info, pump programming, or event details were not available.There were no reports of any adverse pt events or delays in critical therapies while the device was in clinical use.During testing at the user facility, an e360 (screw rotation error) error code was noted.No add'l info was provided.
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