© 2019 Biomed Technologies, inc.

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

Recalled Product:

  • HeartStart MRx Monitor/Defibrillator

  • Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC,...

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