Devices

Device Recall ATLAS II HF Model V367

Model / Serial
all serial codes
Distribution
Nationwide and Internationally: Argentina, Australia, Austria, Barbados, Belgium, Bolivia, Brazil, Canada, Chile, China, Columbia, Costa Rica, Denmark, Dominican Republic, Ecuador, Finland, France, Germany, Hong Kong, Hungary, India, Italy, Japan, Korea, Malaysia,Mexico, Netherlands, New Zealand, Norway, Peru. Poland, Portugal, Republic of Panama, Singapore, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad, United Kingdom, Uruguay and Venezuela.
Product Description
Implantable Cardioverter Defibrillator || ATLAS II+ HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-367
Manufacturer
St Jude Medical CRMD
1 Event
- Recall of Device Recall ATLAS II HF Model V367

Manufacturer

St Jude Medical CRMD

Manufacturer Address
St Jude Medical CRMD, 15900 Valley View Ct, Sylmar CA 91342-3577
Source
USFDA

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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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