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Bad Batch of OxyElite Pro Suspected in Hawaii Liver Injuries

Bad Batch of OxyElite Pro Suspected in Hawaii Liver Injuries

October 4, 2013 — Experts suspect that a “bad batch” of OxyElite Pro could possibly be responsible for an epidemic of liver injury in Hawaii, according to Hawaii News Now.

Although OxyElite Pro is sold throughout the United States, liver injuries have only been reported in Hawaii. The unusual cluster of injuries has fueled speculation that a contaminated shipment may have been sent to Hawaii. High temperatures and improper storage could have changed the effects of the drug.

The injuries occurred between May and September 2013. During that time, the Texas-based manufacturer, USPLabs, sold a re-formulated OxyElite Pro. It is possible that users may have had bad reactions to new ingredients in the product.

Bad Reactions to Re-Formulated OxyElite Pro?

It is unclear whether victims of the outbreak were using new OxyElite Pro or the old formula, which contained DMAA, a powerful stimulant drug that the FDA has been working to take off the market since last year. The crackdown on DMAA began in April 2012, and culminated in July of this year, when the FDA reported that $8 million worth of OxyElite Pro and Jack3d were destroyed by USPLabs. The FDA also reported receiving 86 adverse event reports associated with DMAA, but the reports did not include liver injuries.

What is clear is that the liver injuries in this outbreak are extremely serious. One women became violently ill with nausea, vomiting, and liver failure within weeks of taking OxyElite Pro. Hawaiian health department officials report that at least 32 cases of liver inflammation (hepatitis) and liver failure have occurred, and the only common risk-factor was OxyElite Pro and another dietary supplement, which remains unnamed.

Do I have an OxyElite Pro Lawsuit?

The Schmidt Firm, PLLC is currently accepting OxyElite Pro induced injury cases in all 50 states. If you or somebody you know has been injured by OxyElite Pro, you should contact our lawyers immediately for a free case consultation. Please use the form below to contact our Defective Drug Litigation Group or call toll free 24 hours a day at (866) 920-0753.

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