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.
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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Cronobacter Sakazakii Contamination Results in Recall for Glucerna and Dozens of Other Protein Shakes, Nutritional Supplements, BeveragesCronobacter contamination could lead to serious or even fatal infections August 2, 2022 Russell Maas Add Your CommentsA recall has been issued for Glucerna products, Premier Protein shakes, and dozens of otherย nutritional supplements and beverages manufactured by Lyons Magnus, due to a risk that they may be contaminated with Cronobacter sakazakii, which may cause serious and potentially life-threatening bacterial infections.The FDA announced the supplements recall on July 29, warning that over 50 brand name nutritional products failed to meet commercial sterility specifications and may be contaminated.Cronobacter sakazakii is a rare type of bacteria, often found in dry foods such as infant formula, skimmed milk powder, tea and starches. The bacteria exists in the environment and can survive in very dry conditions, making transmission of the infection possible by touching contaminated surfaces.The infections can be particularly deadly for infants and the elderly, or those with weakened immune systems. In fact, the U.S. Centers for Disease Control and Prevention (CDC) warn the bacteria may cause serious infections or urinary tract infections and poses a heightened mortality risk to those with conditions, such as HIV, organ transplants, or cancer.Contamination with Cronobacter sakazakii recently caused a massive infant formula recall impacting Similac, Alimentum and EleCare products manufactured by Abbott Laboratories at the same Michigan manufacturing plant, which have been linked to hundreds of reported illnesses among babies nationwide in recent months.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 COMPENSATIONLyons Magnus LLC is recalling 53 different nutritional and beverage products due to the potential for microbial contamination, including from the organism Cronobacter sakazakii. The recall notice indicates that while no injuries or illnesses have been reported, the products do not meet the commercial sterility specifications, which puts them at risk of being contaminated with harmful bacteria.The recall impacts protein shakes, cold brew coffee, honey flavored dairy drinks, plant-based protein shakes and a variety of other products that were packed in various formats and sold under 12 different brand names, including Premier Protein, Imperial, MRE, Aloha, Lyons Ready Care, Lyons Barista Style, Pirq, Glucerna, Intelligentsia, Kate Farms, Oatly and Stumptown.Customers are being instructed to stop consuming the products immediately and to properly discard them or return the products to the place of purchase for a refund. Customers with additional questions or concerns regarding the recall are encouraged to contact Lyons Recall Support Center 24/7 at 1-800-627-0557.Cronobacter Baby Formula RecallEarlier this year, Abbott Laboratories issued a Similac, Alimentum and Elecare baby formula recall for certain products made at the companyโs manufacturing facility in Sturgis, Michigan. The recall was issued after Abbott learned about the death of an infant who tested positive for Cronobacter sakazakii after only consuming Similac PM 60/40 powdered formula.Following the recall, the The U.S. Food and Drug Administration (FDA) issued an infant formula warning after Abbott publicly disclosed knowledge of five illnesses, including two deaths after babies consumed infant formula manufactured at the Michigan facility.Just two weeks after the recall, FDA investigators revealed Abbott was aware of illnesses linked to the infant formula several months prior to issuing a recall, raising serious questions about why the Similac, Alimentum and EleCare recall was not announced until February 17, 2022.As a result of the findings, Abbott Laboratories faces a growing number of contaminated Similac formula recall lawsuits filed by families whose children have become ill with Cronobacter sakazakii infections that have resulted in hospitalizations, development of meningitis and other serious injuries or death. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Cronobacter, Dietary Supplement, Food Poisoning, Glucerna, Infection, Supplement RecallMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Carroll August 8, 2022 Does this reaction cause leosons on the skin? 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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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)
Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)
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