Devices

Device Recall VariLase WireFiber

Model / Serial
Lot #'s 550896 and 550898
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution - USA including CT, MA, MN, NY, VA
Product Description
Vari Lase WireFiber Laser Fiber, RED 7137, Rx ONLY, Sterile EO, Vascular Solutions Inc., 6464 Sycamore Court, Minneapolis, MN 55369 || The VARI-LASE WireFiber is indicated for the treatment of varicose veins and varicosities associated with superficial reflux in the Great Saphenous Vein and for treatment of incompetence and reflux of superficial veins in the lower extremity.
Manufacturer
Vascular Solutions, Inc.
1 Event
- Recall of Device Recall VariLase WireFiber

Manufacturer

Vascular Solutions, Inc.

Manufacturer Address
Vascular Solutions, Inc., 6464 Sycamore Ct N, Maple Grove MN 55369-6032
Manufacturer Parent Company (2017)
Teleflex Incorporated
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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