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Créditos
Devices
Device Recall Guidant
Modelo / Serial
Serial numbers 206555, 206557, 206558, 206559, 206560, 206561, 206562, 206525, 206526, 206527, 206528, and 206529
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
3
¿Implante?
Yes
Distribución
Nationwide in the United States and worldwide.
Descripción del producto
Discovery II Multiprogrammable Pacemaker, Model 0981
Manufacturer
Guidant Corp-Cpi Division
1 Event
Retiro De Equipo (Recall) de Device Recall Guidant
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Fabricante
Guidant Corp-Cpi Division
Dirección del fabricante
Guidant Corp-Cpi Division, 4100 N Hamline Ave, St Paul MN 55112-5798
Source
USFDA
45 dispositivos con un nombre similar
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Device Recall Guidant RAPIDO CutAway Guiding Catheter
Modelo / Serial
Lot Number: 0120891 and 0121091
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Nationwide distribution, and Ireland.
Descripción del producto
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
Modelo / Serial
Part number 1007848-15, lot number 7052951
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
3
¿Implante?
Yes
Distribución
Nationwide
Descripción del producto
Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951
Manufacturer
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Device Recall Guidant VITALITY ICD
Modelo / Serial
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
3
¿Implante?
Yes
Distribución
Worldwide
Descripción del producto
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
Modelo / Serial
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
3
¿Implante?
Yes
Distribución
Worldwide
Descripción del producto
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
Modelo / 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
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
3
¿Implante?
Yes
Distribución
Worldwide
Descripción del producto
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
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