Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted March 20, 2007
Recall of Adulterated Sexual Enhancement Supplement
V.MAX is sold nationwide and in the past has also been exported to South Korea and Japan. V.MAX is packaged with an outer box containing three smaller inner boxes each containing five capsules making it a total of 15 capsules per unit.
Consumers who have V.MAX in their possession should stop use immediately. In the event of any adverse side effects due to its consumption, consumers should contact a physician right away. Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.
The company advises that any unused portion be returned to Barodon SF, Inc. for a full purchase price refund by calling (213) 381-8272 for instructions on the return and refund process.
No illnesses have been reported to the company to date in connection with this product.
Barodon SF, Inc. is working closely with the FDA in the recall process to prevent further issues regarding V.MAX.