GlaxoSmithKline received reports from consumers that bottles of Alli (60 mg orlistat capsules) contained capsules and tablets that were not authentic.
San Diego, CA (PRWEB) April 08, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for medical products including weight loss capsules.
As the FDA announced on March 28, GlaxoSmithKline issued a voluntary recall of all Alli weight loss products as they believe that some packages of the product were tampered with and may contain product that is not authentic. It is used for weight loss in overweight people aged 18+ and in combination with a low-fat, reduced calorie diet.
According to the announcement, GlaxoSmithKline received reports from consumers that bottles of Alli (60 mg orlistat capsules) contained capsules and tablets that were not authentic. Moreover, certain bottles had tamper-evident seals and others were missing labels.
Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds, “we are determined to keep an eye on FDA announcements concerning weight loss products and inform the public. For that reason," he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
As the FDA recommends “Consumers who have product they are unsure or concerned about should not use it. Instead, they should call GSK promptly.” And the agency adds, “if they have consumed questionable product, they should also contact their healthcare providers.”
AttorneyOne.com has further information on weight loss products recalls at the website including latest major drug and medical products law news.
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