Device Recall Liko AB Uno Lifts

  • Model / 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
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution --- including USA and country of Canada.
  • Product Description
    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
  • 1 Event

Manufacturer

  • Manufacturer Address
    Liko North America Inc, 122 Grove St, Franklin MA 02038-3159
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Uno 100: S/N 7090001 through 7096200 Uno 101: S/N 10001 through 1000 Production Dates: Manufactured prior to June 26, 2008
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution --- including USA and country of Canada.
  • Product Description
    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