Devices

Device Recall Guidant VITALITY AVT

Model / Serial
model A155, serial numbers: 113567, 113568, 113569, 113570, 113572, 113574, 113585, 113586, 113587, 113591, 113612, 113613, 113616, 113617, 113618, 113619, 113620, 113621, 113623, 113624, 113626, 113627, 113628, 113629, 113631, 113633, 113635, 113637, 113639, 113640, 113641, 113654, 113659, 113660, 113672, 113674, 113675, 113676, 113678, 113679, 113680, 113681, 113682, 113684, 113686, 113687, 113690, 113693, 113694, 113695, 113696, 113778, 113779, 113781, 113783, 113784, 113789, 113791, 113792, 113814, 113908, 113910, 113912, 113913, 113914, 114083
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide including Puerto Rico. Worldwide, including Argentina, Belgium, Canada, Denmark, France, Germany, Greece, Ireland, Italy, Netherlands, New Zealand, Portugal, Spain, Syrian Arab Republic, United Arab Emirates
Product Description
VITALITY AVT, model A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
Manufacturer
Boston Scientific CRM Corp
1 Event
- Recall of Device Recall Guidant VITALITY AVT

Manufacturer

Boston Scientific CRM Corp

Manufacturer Address
Boston Scientific CRM Corp, 4100 Hamline Ave N, Saint Paul MN 55112-5700
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Guidant VITALITY AVT ICD

Model / Serial
all serial numbers
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
worldwide. To the US and OUS countries to include: Argentina, Australia, Austria, Belgium, Canada, Chile, Cyprus, Denmark, France, Germany, Guadeloupe, Hong Kong, Ireland, Israel, Italy, Japan, Jordan, Lebanon, Luxembourg, Netherlands, New Zealand, Norway, Portugal, Saudi Arabia, Slovenia, Spain, Sweden, Switzerland, Syrian Arab Republic, Turkey, US - Virgin Islands and United Kingdom.
Product Description
VITALITY AVT, model A135 and model A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. Sterilized using gaseous ethylene oxide. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
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

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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