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.
Apple Juice Arsenic Recall Expanded to Include Weis, Walgreens, BJ’s and Aldi’s Brand ProductsWalmart Great Value apple juice recall now also includes Refresco products distributed through other retailers. September 12, 2024 Michael Adams Add Your CommentsFollowing a Walmart apple juice recall issued late last month, due to high levels of the known carcinogen arsenic, Refresco Beverages has initiated an additional voluntary recall that impacts other versions of its juices sold at Weis, Walgreens, BJ’s and Aldi’s stores.Unlike organic arsenic which can quickly pass through the human body and is generally not harmful, inorganic arsenic found in the apple juice is a toxic substance, especially when an individual is exposed to it at high levels or over long periods of time. Side effects of exposure have been linked to a number of serious adverse health conditions, including cancer, heart disease and death.The presence of inorganic arsenic in apple juice products is particularly concerning, since the compound can be extremely harmful for children, impacting brain development and IQ, as well as potentially leading to long term cancer risks.Refresco Beverages issued the expanded apple juice arsenic recall notice on September 9, indicating that the problems not only impact Great Value apple juice sold at Walmart stores, but also impacts store brands sold by Weis, Walgreens, BJ’s and Aldi’s, including Nice!, Urban Meadow, Natures Nectar, Wellsley Farms, Solevita, Clover Valley and Tropical Delight apple juice brands.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 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 COMPENSATIONLike the previous apple juice recall, the U.S. Food and Drug Administration (FDA) has also categorized this expansion as a Class II recall, meaning that consumption of the beverages will not likely lead to serious health consequences, but may negatively impact individuals’ health over a shorter time period.However, consumers should keep in mind that the amount of arsenic in these beverages could still be nearly 33% higher than guidance levels set by the FDA. Acceptable amounts of inorganic arsenic in foods and drinks were lowered by the FDA in mid-2023, after toxic levels of arsenic and other metals were found in a number of baby food products, raising concerns about the impact of those products on children in particular.Refresco Beverages Apple Juice RecallThe current recall now affects 141,298 cases of apple juice sold at various retailers under different brand names, including Great Value, Market Basket, Nice!, Weis, Urban Meadow, Natures Nectar, Wellesley Farms, Solevita, Clover Valley and Tropical Delight, all of which were made with tainted concentrate from an outside supplier.The products were sold in Alabama, Florida, Georgia, Indiana, Kentucky, Maine, Maryland, Massachusetts, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, South Carolina, Virginia and Wisconsin.The affected cases include the following products, best by dates and product codes:Great Value 8 oz. bottles, with best if used by dates of December 26, 2024 and December 27, 2024, and product code CT89-6Great Value 96 oz. bottles, with best if used by dates of December 26, 2024, December 27, 2024 and December 28, 2024, and product code CT89-5Market Basket 100% apple juice, with sell by date of March 25, 2025, and product code CT89-1Nice! 100% apple juice, with best by date of March 25, 2025, and product code CT89-1Weis 100% apple juice, with best by date of March 25, 2025, and product code CT89-1Urban Meadow 100% apple juice, with best by date of March 26, 2025, and product code CT89-1Natures Nectar 100% apple juice, with best by date of March 26, 2025 and March 27, 2025, and product code CT89-4Wellsley Farms 100% apple juice, with best by date of March 26, 2025, and product code CT89-5Solevita 100% apple juice, with best by date of March 27, 2025, and product code CT89-4Clover Valley 100% apple juice, with best by date of March 27, 2025, and product code CT89-4Tropical Delight 100% apple juice, with best by date of July 25, 2025Refresco Beverages says that no incidents or injuries have yet been reported as a result of the inorganic arsenic in apple juice products they sold. However, they are encouraging all customers and consumers to use FDA recall information to determine if they are still in possession of the affected beverages.“The safety of consumers is always our top priority,” Refresco said. “(O)ut of an abundance of caution, we voluntarily initiated a recall of some select lots of 100% apple juice products produced using supplier provided concentrate when we became aware that previously manufactured product contained inorganic arsenic slightly above the FDA’s 10 ppb (parts per billion) action level as set by the FDA in June 2023 in the FDA Final Guidance to Industry on Action Level for Inorganic Arsenic in Apple Juice.”Retail distribution centers that believe they are still in possession of the affected apple juice can call the company at 1-888-260-3776 and press 2. Consumers with questions are encouraged to call 1-888-260-3776 and press 3. Written by: Michael AdamsSenior Editor & JournalistMichael Adams is a senior editor and legal journalist at AboutLawsuits.com with over 20 years of experience covering financial, legal, and consumer protection issues. He previously held editorial leadership roles at Forbes Advisor and contributes original reporting on class actions, cybersecurity litigation, and emerging lawsuits impacting consumers. Tags: Aldi, Apple Juice Recall, Arsenic, BJ, BJs, Great Value Apple Juice, Inorganic Arsenic, Walgreens, Walmart, Weis Image Credit: HitraMore Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer ‘Dusky Metal Disease’ June 5, 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 3 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 4 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Woman’s CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 5 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamics’ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Woman’s Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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