Devices

Device Recall Battery Pack

  • Modelo / Serial
    Model Number 915 Manufacturing Lot Number 45-03
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The recalled product was distributed nationwide and internationally to the folllowing states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WI, WV . In regards to foreign accounts, the product was distributed to Canada and British Columbia.
  • Descripción del producto
    Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter.
  • Manufacturer
    Respironics, Inc.
  • 1 Event

Fabricante

Respironics, Inc.
  • Dirección del fabricante
    Respironics, Inc., 1010 Murry Ridge Ln, Murrysville PA 15668
  • Source
    USFDA