Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences

spacer.gif (43 bytes)

FOOD AND DRUG ADMINISTRATION
FOR IMMEDIATE RELEASE

Consumer Media: 888-Info-FDA
April 28, 1999

GH Revitalizer Oral Liquid Recalled

PRODUCT
GH Revitalizer Oral Liquid (2-(3H)- Furanone dihydro), OTC in 32 fluid ounce bottles, labeled for use for bodybuilding and sleep purposes. Recall #D-186-9.

CODE
All lot codes.

MANUFACTURER
GH Revitalizer, also known as HI-IR Industries, Orange Park, Florida.

RECALLED BY
Manufacturer, by letter dated February 9, 1999. Firm-initiated recall ongoing. See also FDA talk paper T99-5 dated January 21, 1999.

DISTRIBUTION
Nationwide.

QUANTITY
Approximately 3,600 bottles were distributed; firm estimates none remains on the market.

REASON
Product is an unapproved new drug.

 

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.