Guidant VITALITY® 2 Defibrillator Recall

On June 23, 2006 Guidant Corporation in association with the U.S. Food & Drug Administration (FDA) issued a recall of a large number of VITALITY® 2 defibrillators.

Guidant Corporation Comments: a limited number of these devices contain a part (component) that on rare occasion may prevent the device from delivering therapy, or cause the device’s battery to run down before it should.

Do I Have a Guidant VITALITY® 2 Recall Lawsuit?

If you or a loved one have a Guidant VITALITY® 2 defibrillator, regardless of whether or not you have experienced device malfunctions or failure, you should contact us immediately. You may be entitled to compensation and we can help.

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