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Hydroxycut Litigation Over Recalled Supplement Consolidated in MDL October 8, 2009 AboutLawsuits Add Your CommentsThe U.S. Judicial Panel on Multidistrict Litigation has ordered that the federal Hydroxycut litigation, involving claims for liver damage and other health problems allegedly caused by the recalled dietary supplement, will be consolidated and centralized for pretrial proceedings in the U.S. District Court for the Southern District of California.According to an order issued October 6, there are at least 16 Hydroxycut lawsuits pending against the manufacturer, Iovate Health Sciences, in 12 different federal districts throughout the United States. Following a hearing last month, the panel determined that all of the cases involve sufficiently similar questions of fact to justify consolidation into an MDL, or multidistrict litigation. There are also six other cases which were not included in the initial order, but which the panel said may be transferred later as tag-along cases.Hydroxycut is a dietary supplement and weight-loss aid that was recalled on May 1, 2009, after the FDA identified a number of reports where users suffered serious and potentially life-theatening liver damage. The FDA also reported that use of Hydroxycut was linked to reports of seizures, heart problems and a rare muscle damaging condition known as rhabdomyolysis.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAll of the cases in the litigation over Hydroxycut involve allegations that Iovate Health Sciences failed to adequately research their weight-loss products or warn about potential side effects prior to issuing the Hydroxycut recall.An MDL is designed to avoid inconsistent pretrial rulings in similar cases spread throughout the country, eliminate repeat discovery on issues that are common to all cases and to serve the convenience of the parties, the witnesses and the court. While the cases will be consolidated for pretrial litigation, each Hydroxycut claim will remain an individual lawsuit and if a settlement or other resolution is not reached, they may be returned back to the jurisdiction where they were originally filed for trial.Some plaintiffs sought to avoid having their cases included in an MDL, saying the facts in their cases were too disparate. Others sought for the MDL to be created in a different federal district, but the judicial panel overrode those objections and placed the cases under U.S. District Judge Barry Ted Moskowitz, saying that there were already several cases in his court, and he is a judge experienced with handling complex multi-district litigation. Tags: California, Dietary Supplement, Hydroxycut, Hydroxycut Recall, Iovate, Liver Damage, Rhabdomyolysis Image Credit: |More Lawsuit Stories FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses August 19, 2026 AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users August 19, 2026 Anti-Seizure Drugs Linked to a Quarter of Stevens-Johnson Syndrome Cases August 19, 2026 1 Comments Tonya November 8, 2010 I used Hydroxycut for 7 years and in that time I was hospitalized for elevated liver enzymes at 1297, kidney failure, and I am still extremely sick. At the time my doctors could not give me a reason for all of my medical problems, now it makes perfect sense. Whatever Iovate Health Sciences has to pay will never be enough for all the suffering they caused. 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This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: today)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: yesterday)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026) Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: 2 days ago)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)
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