Q: Have there been any adverse health consequences from this issue?
A: In all cases reported to date, the problem has been detected by the FR2+ during a periodic self-test or a battery insertion test. There have been no reported incidents of the problem during emergency use of the AED, and no injuries to users or patients. Our investigation has determined that adverse health consequences are very unlikely as a result of this issue. The majority of devices subject to this recall are not expected to experience the problem. However, the potential for this failure does not meet Philips performance expectations.