Devices

Device Recall Liko AB Uno Lifts

  • Modelo / Serial
    Uno 100: S/N 7090001 through 7096200 Uno 101: S/N 10001 through 1000 Production Dates: Manufactured prior to June 26, 2008
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution --- including USA and country of Canada.
  • Descripción del producto
    Liko AB Uno Lifts, Powered (non-AC) Patient Lift: || Uno 100 EM/EE: S/N 7090001 through 7096200 || Uno 101: S/N 10001 through 11000 || Production Dates: Manufactured prior to June 26, 2008 || Uno 100 and 102 are battery powered mobile lifts, designed to be used in most of the common lifting situations, for example transfers between bed and wheelchair, to and from the toilet and bathtub or for lifting to and from the floor.
  • Manufacturer
    Liko North America Inc
  • 1 Event

Fabricante

Liko North America Inc
  • Dirección del fabricante
    Liko North America Inc, 122 Grove St, Franklin MA 02038-3159
  • Source
    USFDA

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Device Recall Liko AB Uno Lifts
  • Modelo / Serial
    Old Uno 102: S/N 20001 through 21300 New Uno 102: S/N 30001 through 48100 Production Dates: Manufactured prior to June 26, 2008
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution --- including USA and country of Canada.
  • Descripción del producto
    Liko AB Uno Lifts, Powered (non-AC) Patient Lift: || Old Uno 102: S/N 20001 through 21300 || New Uno 102 EM/EE/ES: S/N 30001 through 48100 || Production Dates: Manufactured prior to June 26, 2008 || Uno 100 and 102 are battery powered mobile lifts, designed to be used in most of the common lifting situations, for example transfers between bed and wheelchair, to and from the toilet and bathtub or for lifting to and from the floor.
  • Manufacturer
    Liko North America Inc