Devices

Device Recall Powerlink (R) System with IntuiTrak Delivery System

Model / Serial
MODEL NUMBER 34-34-80LE, LOTS W09-2967 AND W09-3000.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
Product Description
Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80LE, LOTS W09-2967 AND W09-3000.
Manufacturer
Endologix Inc
1 Event
- Recall of Device Recall Powerlink (R) System with IntuiTrak Delivery System

Manufacturer

Endologix Inc

Manufacturer Address
Endologix Inc, 11 Studebaker, Irvine CA 92618-2013
Source
USFDA

One device with a similar name

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Device Recall Powerlink (R) System with IntuiTrak Delivery System

Model / Serial
MODEL NUMBER 34-34-80L, LOTS W09-2966 AND W09-2998.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
Product Description
Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80L, LOTS W09-2966 AND W09-2998.
Manufacturer
Endologix Inc

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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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