Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Nearly 1,000 Reglan Lawsuits Now Pending in New Jersey State Court April 7, 2011 Staff Writers Add Your CommentsThe New Jersey state court system has seen a sharp increase in the number of Reglan tardive dykinesia lawsuits filed over the past few months, as many complaints were filed in advance of a possible Reglan statute of limitations deadline for the state in February.ย ย According to a case list released on April 2, there were 983 Reglan complaints centralized before Judge Carol Higbee in Atlantic County, New Jersey for coordinated handling during pretrial litigation. All but about 120 of those lawsuits were filed since February 1.Each Reglan lawsuit involves similar allegations, that the manufacturers of the name brand gastrointestinal drug and generic Reglan equivalents failed to adequately warn users or the medical community about the potential risk of tardive dyskinesia from Reglan. Long term use of Reglan has been linked to an increased risk of the movement disorder, which is associated with repetitive and involuntary movements, particularly involving the lower face and limbs.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 COMPENSATIONJust over two years ago, in February 2009, the FDA announced that the manufacturers of Reglan and generic metoclopramide drugs were being required to add a โblack boxโ warning, alerting patients and doctors to the increased risk of tardive dyskinesia side effects when Reglan is used at higher doses or over a long period of time.New Jersey is among about half of the states in the country that require claims to be filed within two years of when a cause of action accrues, which may be interpreted to be the date that the new warnings were announced. However, new lawsuits continue to be reviewed by Reglan lawyers for individuals who may have additional time to bring a case based on the statute of limitations in their state.Reglan, which is known generically as metoclopramide, is approved for the short-term treatment of gastrointestinal disorders like diabetic gastroparesis, gastroesphageal reflux (GERD) and delayed gastric emptying. However, it is often prescribed for longer periods of time due to the often chronic persistence of those ailments, which has left many users with the movement disorder tardive dyskinesia.Symptoms of tardive dyskinesia can include grimacing, chewing, smacking of lips, rapid eye movements and impaired finger movements. There is no known effective treatment of the socially debilitating disorder, and the involuntary movements can be permanent, persisting even after use of the drug has stopped.Throughout the United States, it is unknown exactly how many cases are involved in the Reglan litigation, as there is no centralized management for the cases filed in federal court and cases are pending in a number of different state courts. Tags: Metoclopramide, New Jersey, Reglan, Tardive DyskinesiaMore Lawsuit Stories DraftKings Gambling Lawsuit Alleges Illegal Scheme Fueled Addiction October 27, 2026 Snapchat Child Sexual Abuse Lawsuit Alleges Predator Targeted 9-Year-Old Girl October 27, 2026 Olympus Scope Problems Lead to FDA Import Warning October 27, 2026 3 Comments Confused May 21, 2014 What is so hard to come to a decision on this matter? The Generic Brand of Reglan contains the exact same medication in it that Reglan does which causes Tardive Dyskinesia! It seems to be a NO BRAINER to me! For people who can not afford the brand name drug, such as people on Medicaid and such, the Generic Brand is ALL that their Insurance will Pay for. IT IS NOT THEIR FAULT IS IT? As it has been states , 70% of the people whom took Reglan received the Generic Brand!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! WAKE UP AND RECOGNIZE AND JUST ADMIT A MISTAKE HAS BEEN MADE BY THE DRUG MAKERS AND SO THEY SHOULD HAVE TO PAY FOR IT AND NOT JUST TURN THEIR HEADS ON THE PEOPLE AFFECTED BY THIS OR ELSE JUST BAN GENERIC BRANDS ALL TOGETHER !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! Jenniflower73 June 13, 2011 WORSE DRUG EVER – IT HAS TAKEN MY MOMS FREEDOM FROM HER!! Not to mention, her grand babies will never know the true strong woman she is. She has ALL the side effects from this and all I can do is watch… I miss my MOM – Jamie May 11, 2011 i have been taking up to 4 reglans a day and i am 34 i started at age 20 i will say …. no wonder i have i movements all the time and my arm shakes ..wow URLThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. 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