Device Recall BARD DORADO

Manufacturer

  • Manufacturer Address
    Bard Peripheral Vascular Inc, 1625 W 3rd St, Tempe AZ 85281-2438
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

14 devices with a similar name

Learn more about the data here

  • Model / Serial
    LOT NUMBERS: 93DT0019, 93DT0050, 93DT0205, 93FT0310
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135412
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93DT0101, 93DT0103, 93FT0034, 93FT0293, 93JT0068
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135415
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93DT0104, 93DT0105, 93GT0108
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135417
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93GT0144
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135420
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93FT0028
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135512
  • Manufacturer
9 more