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November 30, 1999

Invigorate Liquid Drink Recalled

New York, NY (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Invigorate International is recalling certain Invigorate(tm) Liquid Drink sold in 32 fluid ounce plastic bottles because the product is a drug that has not been approved by the FDA.

This Class I recall was initiated by Cabot Industries, LLC on June 1, 1999 by letter.  This is the first notice the FDA has issued to the general public of the recall.

An unknown quantify of the recalled product was distributed in New York, New Jersey, Massachusetts, Pennsylvania, Maryland, Virginia, Ohio, South Carolina, Florida, Alabama, Mississippi, Michigan, Illinois, Kansas, Colorado. 

The product label declares as an ingredient “2 (3H) “2(3H) Furanone Di-hydro”, which is also known as gammabutyrolactone (GBL). The supplement which stimulates the body’s own production of human growth hormone and as a sleep aid which “will induce deep invigorating sleep that will last 3-4 hours.This recall affects all codes remaining on the market.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.