H10:a return material authorization had been provided to the customer for the return of the fetal spiral electrode.Only the needle was available, the main body of the fetal spiral electrode was discarded.The entire fetal spiral is needed for a proper evaluation.No material has been received in andover; therefore, an evaluation was not completed.The needle coil was removed from the baby's scalp with a pair of forceps.There were no further details of the infant¿s condition.Submission of a report does not constitute an admission that medical personnel, user facility, importer, distributor, manufacturer, or product caused or contributed to the event.
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