The customer contact reported an error code of e630 (screw rotation error).The device was returned to the biomedical department for an unspecified reason.No tracking info was provided; therefore, specific pt info, device 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, the device displayed error 630 (screw rotation error).No add'l info was provided.
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