It was reported that the device's therapy label is peeling from device.The device was reported to be in use on a patient, but no adverse event to patient or user was reported.The manufacturer's authorized field service engineer (fse) evaluated the device and confirmed the reported problem.Upon conclusion of the evaluation, it was determined that this was a malfunction of the therapy label, which was replaced, and the device was returned to full functionality.The device remains at the customer site and no further evaluation is warranted at this time.
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