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.
Nature Made Vitamin Recall Issued Over Bacterial Contamination Hits Giant, Martin’s Stores June 9, 2016 Russell Maas Add Your CommentsSeveral lots of “Nature Made” dietary supplements sold at Giant and Martinโs Food Markets have been recalled, due to a risk that they may be contaminated with micro-organisms that can pose serious and sometimes life threatening health consequences.ย The Pharmative Nature Made vitamin recall was announced by the FDA on June 8, after it was discovered that proper contamination testing was not performed on the products. To date, no illnesses have been reported in connection to the recalled vitamins.Pharmative LLC issued a press release on their companyโs website, indicating that the products were not put through the correct, vigorous testing process used to identify contamination. Without the products at least being put through standard testing, Pharmative LLC stated the company cannot be certain the products are not contaminated with salmonella, staphylococcus aureus, yeast or mold.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 COMPENSATIONAlthough no bacterium has been found at the facility or in any of the products, the FDA and Pharmative LLC are recalling all of the impacted products from Martinโs and Giant Food Stores where the supplements were sold.All of the potential contaminants pose health consequences to consumers, especially those with weakened immune systems such as children or the elderly.Salmonella, which is one of the most common bacterial foodborne illnesses recorded can cause life-threatening infections to the elderly and children, and has been known to cause miscarriages or stillbirths for pregnant women. The symptoms of the illness involve abdomen pain, headaches, diarrhea, and dehydration lasting about four to seven days.Similarly, staphylococcus aureus infections cause many flu-like symptoms on a much more severe scale that, if left untreated, could develop into intense headaches, muscle cramping and transient changes in blood pressure and pulsed rates.Ingestion of the dietary products containing mold or yeast may cause mild bowel discomfort, however in small doses the consumerโs stomach acid destroys mold once it is contacted. Individuals with mold allergies may be at an increased risk for additional symptoms triggered by the immune system including wheezing, itchy and runny nose, watery eyes, and rashes or irritations of the skin usually requiring medical attention.Included in the recall are Nature Made Adult Gummies Multi with Lot # 1196066, Nature Made Adult Gummies Multi with Lot # 1196071 and 1205052, Nature Made Adult Gummies Multi + Omega 3s with Lot # 1173600, Nature Made Adult Gummies Multi for Her plus Omega-3s with Lot # 1196050, Nature Made Adult Gummies Hair, Skin, Nails, with Lot # 1198437, Nature Made Adult Gummies Hair, Skin, Nails, 150 count with Lot # 1198438, Nature Made Vitamin D 1000 IU Tablets with Lot #s 1147550, 1174782 and 1176755, Nature Made Vitamin D 1000 IU Tablets with Lot #s 1140172, 1175637 and 1176756, Nature Made Vitamin D 1000 IU Tablets with Lot # 1147978, Nature Made Super B Complex w/ C & Folic Acid Tablets with Lot # 1173779, Nature Made Super B Complex w/ C & Folic Acid Tablets with Lot #s 1173146 and 1204001.Pharmavite announced the company investigators identified the cause of the error and are taking the necessary steps to prevent the error from occurring in the future. For a full list of the recalled items, including vitamin counts and UPC codes please visit the FDAโs recall notice.Customers are being asked to stop using the recalled dietary supplements and discard any remaining products and return the receipt to any Giant or Martinโs Food Market for a full refund. For additional recall information or further questions customers may contact Giant/Martinโs Customer Service at 888-814-4268. 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: Dietary Supplement, Food Poisoning, Giant, Martin's, Mold, Salmonella, Staph InfectionMore 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 0 Comments NameThis 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. 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: 3 days ago)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: 4 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: 5 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)
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