HeartStart MRx recall

Phillips is recalling the HeartStart MRx Monitor/Defibrillator due to electrical and battery connection issues that may prevent the device from powering up, charging, and delivering an electrical shock therapy. The device may also unexpectedly stop pacing.  The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

For complete details: https://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm548491.htm