Company: Philips Medical Systems, Inc. Date of Enforcement Report 4/16/2014 Class lI: PRODUCT Philips HeartStart XL+ Defibrillator/Monitor with system software version B.00.00 or B.00.01 installed Model: 861290, automatic external defibrillator. Recall Number Z-1438-2014 REASON Software communication failure may occur on the HeartStart XL+ locking the user out of clinical mode and possibly causing a delay...Read More