Philips received a complaint on the efficia dfm100 defibrillator indicating that the device was dropped and did not pass the test.There was no patient involvement.The philips bench evaluated the device and determined the therapy receptacle was defective.The philips bench replaced the therapy receptacle resolving the reported issue.Based on the information available and the testing conducted, the cause of the reported problem was a malfunction of the therapy receptacle.The reported problem was confirmed.The philips bench replaced the therapy receptacle resolving the reported issue.It has been concluded that no further action is required at this time.The efficia dfm100 defibrillator, model# 866199, is substantially similar to the heartstart xl+ defibrillator (model # 861290) and will be reported in the united states under device model # 861290.
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