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: 93FT0152
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135712
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93DT0146, 93DT0175, 93IT0211, 93IT0211
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135715
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93FT0217
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135717
  • Manufacturer
  • Model / Serial
    LOT NUMBERS: 93FT0218, 93HT0155
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135720
  • Manufacturer
  • 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
9 more