On July 13 , 2011 - United States FDA and Global Wellness, LLC. Hollywood, FL
expanded its voluntary nationwide recall of VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN to the consumer level to include lot A032111. The product was distributed throughout the U.S. Puerto Rico, Barbados, and Canada to internet and retail consumers. The product is distributed as a bottle containing six (6) blue colored capsules per package. The label on the packaging lists the company name Global
Wellness, LLC, Hollywood Florida. Lot numbers #809013, 806030, and A032111 are covered in this recall.

On March 4, 2011 FDA notified healthcare professionals and patients of an increased risk of development of cleft lip and/or cleft palate (oral clefts) in infants born to women treated with Topamax (topiramate) during pregnancy.

On March 8, 2011 FDA notified healthcare professionals of serious health problems that have been reported in premature babies receiving Kaletra (lopinavir/ritonavir) oral solution.