The device was returned to the service center for a report from the customer contact that the device was received in the biomedical department with an unsigned note that stated, "malfunction message." however, during verification testing at the ser center an e630 (screw rotation error) error code was noted.
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During testing, the device passed testing.An e630 (screw rotation error) error code was noted in the device history but was not duplicated during testing.Although the device passed testing, the device has been identified a part of a product recall.This report represents all the info known by the reporter upon query by hospira personnel.
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