Devices

Device Recall VENTAK, PRIZM 2 DR ICD

Model / Serial
263958, 264039, 264055, 264058, 264059, 264060, 264064, 264066, 264069, 264070, 264112, 264117 and 264119
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
CA, IL, MI, MO, OR and PA
Product Description
PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator. Contents have been Sterilized with gaseous ethylene oxide. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
Manufacturer
Guidant Corporation
1 Event
- Recall of Device Recall VENTAK, PRIZM 2 DR ICD

Manufacturer

Guidant Corporation

Manufacturer Address
Guidant Corporation, 4100 Hamline Ave N, Saint Paul MN 55112-5700
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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