While performing onsite service of the device, it was identified by an authorized field service engineer that the labeling for the unit was damaged.The customer requested that an authorized field service engineer (fse) be dispatched to the customer site.Upon evaluation of the device, it was discovered that the labeling for the unit was damaged and required replacement.Based on the conclusion of the evaluation, it was determined that this was a malfunction of the therapy label.The therapy label was replaced to resolve the noted damage.The device remains at the customer site.There is no indication of a systemic problem.No further investigation or action is warranted.
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