Devices

Device Recall Guidant

  • Model / Serial
    Lots 4011451, 4012151, 4012451, 4020451, 4020651, 4021251, 4021751, 4022351, and 4022551
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide in the United States.
  • Product Description
    Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 54 cm, Coronary Sinus - Multi-Purpose Tip Shape, CS-MP, REF 7300
  • Manufacturer
    Guidant Corp-Cpi Division
  • 1 Event

Manufacturer

Guidant Corp-Cpi Division
  • Manufacturer Address
    Guidant Corp-Cpi Division, 4100 Hamline Ave N, Saint Paul MN 55112-5700
  • Source
    USFDA

45 devices with a similar name

Learn more about the data here

Device Recall Guidant RAPIDO CutAway Guiding Catheter
  • Model / Serial
    Lot Number: 0120891 and 0121091
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide distribution, and Ireland.
  • Product Description
    Guidant RAPIDO Cut-Away Guiding Catheter, 6F. || Part Numbers: 66676-201 and 667552-100. || For use in cardiac diagnostic and therapeutic procedures.
  • Manufacturer
    Abbott Vascular
Device Recall Guidant MultiLink RX Vision
Device Recall Guidant VITALITY ICD
  • Model / Serial
  • Product Classification
    Cardiovascular Devices
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Worldwide
  • Product Description
    Guidant VITALITY VR/DR, Implantable Cardioverter Defibrillator, ICD, Models 1870 and 1871. Guidant VITALITY DR+, Implantable Cardioverter Defibrillator, ICD, Model 1872.
  • Manufacturer
    Boston Scientific CRM Corp
Device Recall Guidant VITALITY AVT ICD
  • Model / Serial
  • Product Classification
    Cardiovascular Devices
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Worldwide
  • Product Description
    Guidant VITALITY AVT, Models A135 and A155. Implantable Cardioverter Defibrillator, ICD. Atrial and Ventricular Therapies. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
  • Manufacturer
    Boston Scientific CRM Corp
Device Recall Guidant ASSURE ICD
  • Model / Serial
    Model B301: B301/100002, B301/100003, B301/100004, B301/100006, B301/100007, B301/100008, B301/100010, B301/100012, B301/100013, B301/100014, B301/100016, B301/100019, B301/100020, B301/100021, B301/100022, B301/100024, B301/100025, B301/100027, B301/100030, B301/100031, B301/100032, B301/100034, B301/100037, B301/100039, B301/100043, B301/100044, B301/100045, B301/100046, B301/100048, B301/100050, B301/100051, B301/100053, B301/100054, B301/100056, B301/100062, B301/100063, B301/100064, B301/100067, B301/100069, B301/100070, B301/100073, B301/100074, B301/100075, B301/100076, B301/100079, B301/100080, B301/100081, B301/100082, B301/100083, B301/100084, B301/100087, B301/100088, B301/100089, B301/100090, B301/100091, B301/100092, B301/100094, B301/100096, B301/100099, B301/100100, B301/100101, B301/100102, B301/100103, B301/100104, B301/100105, B301/100106, B301/100108, B301/100111, B301/100112, B301/100113, B301/100114, B301/100115, B301/100116, B301/100117, B301/100118, B301/100120, B301/100122, B301/100125, B301/100126, B301/100128, B301/100129, B301/100130, B301/100131, B301/100132, B301/100134, B301/100135, B301/100136, B301/100137, B301/100139, B301/100140, B301/100141, B301/100142, B301/100143, B301/100144, B301/100145, B301/100146, B301/100147, B301/100148, B301/100149, B301/100153, B301/100154, B301/100155, B301/100158, B301/100159, B301/100161, B301/100162, B301/100164, B301/100165, B301/100166, B301/100167, B301/100169, B301/100170, B301/100172, B301/100173, B301/100174, B301/100176, B301/100180, B301/100181, B301/100182, B301/100183, B301/100185, B301/100186, B301/100187, B301/100188, B301/100189, B301/100191, B301/100193, B301/100194, B301/100195, B301/100196, B301/100197, B301/100200, B301/100203, B301/100204, B301/100205, B301/100206, B301/100208, B301/100209, B301/100210, B301/100211, B301/100213, B301/100215, B301/100216, B301/100218, B301/100221, B301/100222, B301/100223, B301/100224, B301/100226, B301/100227, B301/100230, B301/100234, B301/100235, B301/100236, B301/100238, B301/100239, B301/100242, B301/100243, B301/100244, B301/100245, B301/100247, B301/100249, B301/100253, B301/100255, B301/100258, B301/100260, B301/100264, B301/100271, B301/100272, B301/100273, B301/100279, B301/100280, B301/100285, B301/100288, B301/100290, B301/100293, B301/100298, B301/100315, B301/100317, B301/100318
  • Product Classification
    Cardiovascular Devices
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    Worldwide
  • Product Description
    Guidant ASSURE, Model B301, Implantable Cardioverter Defibrillator, ICD. (This model is not available in the USA) Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
  • Manufacturer
    Boston Scientific CRM Corp
40 more