November 30, 1999Invigorate Liquid
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,
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 bodys 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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