Archer Super Stiff Guidewire

  • Model / Serial
    Model: ARCSJ200WLot: GFWC1124; GFWC1506; GFWC2138; GFWC2652; GFWC2653; GFWD0353; GFWD0881; GFWD0882; GFWD2048; GFWD2049; GFWD2050; GFWD2051; GFWD2052; GFWE0743; GFWE0744; GFWE0745; GFWE0746; GFWE0747; GFWE3710; GFWE4272; GFWE4273; GFWE4274; GFWE4275; GFWF0143; GFWF0144; GFWF0147; GFWF0148; GFWF0149; GFWG0428; GFWG0429; GFWG0430; GFWG0431; GFWG0432; GFWG0433; GFWG0434; GFWH0333; GFWH0334; GFWH0335; GFWH0336; GFWH0337; GFWH0338; GFWI0190; GFWI0191; GFWI0192; GFWI0193; GFWI0194; GFWI0195; GFWJ0027; GFWJ0028; GFWJ0029; GFWJ2454; GFWJ2455; GFWJ2456; GFWJ2457; GFWJ2458; GFWK1910; GFWK1911; GFWL0370; GFWL2571; GFWL2572; GFXA0224;Model: ARCSJ260WLot: GFWC1501; GFWC1502; GFWC1503; GFWD0883; GFWD0884; GFWD3256; GFWE0752; GFWE0753; GFWE3711; GFWF0145; GFWF0150; GFWG0425; GFWG0426; GFWG0427; GFWH0344; GFWH0345; GFWI0201; GFWI0202; GFWI0203; GFWJ0418; GFWJ0419; GFWJ0420; GFWJ2461; GFWJ2462; GFWJ2464; GFWJ2465; GFWL0368; GFWL0369; GFWL0415; GFWL0416; GFXA0219; GFXA0220; GFXA0221; GFXA0222;Model: ARCDJ260WLot: GFWC1507; GFWC1508; GFWD0885; GFWE0750; GFWE0751; GFWF0142; GFWF0146; GFWG0423; GFWG0424; GFWH0331; GFWH0332; GFWI0186; GFWI0187; GFWI0188; GFWJ2449; GFWJ2450; GFWJ2451; GFWJ2452; GFWK1844
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    ALIMSA

3 devices with a similar name

Learn more about the data here

  • Model / Serial
    Lot number GFWA0387
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution-USA including the states of FL, OH, and MN and the countries of Belgium, France Germany, Netherlands, Turkey, and United Kingdom.
  • Product Description
    Medtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm), Model ARCSJ200W. || Intended to facilitate catheter placement and exchange during procedures in the aorta.
  • Manufacturer
  • Model / Serial
    ARCSJ200W, ARCSJ260W, ARCDJ260W
  • Product Description
    MD: Cardiac catheter guidewire, single-use
  • Manufacturer