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.
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
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.
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.
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.
Bottled Water Recall Expanded Due to Contaminated Water Source June 24, 2015 Russell Maas Add Your CommentsAt least 14 brands of bottled water distributed throughout 15 different states in the U.S. are being recalled, after an operator failed to report evidence of E.coli bacteria contamination at the Pennsylvania spring source.ย Niagara Bottling has announced a bottled Spring Water recall expansion that includes certain brands collected from two Pennsylvania plants, after learning the spring source tested positive for E.coli contamination, posing a sickness hazard to consumers. To date, Niagara has not received any reports of illness in relation to the consumption of the recalled spring water.The Niagara Spring Water recall originally began on June 20, when Wegmanโs recalled certain “Food You Feel Good About” bottled water products due to a risk of E.coli bacteria. On June 22, Niagara Bottling added 13 more brands that may be impacted, out of an abundance of caution.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 COMPENSATIONAccording to a statement on the Niagra Bottling company website, there has been a great deal of miscommunication and misinformation between the company and the Pennsylvania plant about the contamination, prompting the company to recall all products collected from that specific spring source.Niagara Bottling reported that one of its suppliers, Far Away Springs, which run two separate Pennsylvania plants, failed to notify Niagara of a positive E.coli test result in the spring source. Niagara spokesman Stan Bratskeir, reported that Far Away Springs notified the Department of Environmental Control and the Department of Agriculture of the positive test result but failed to report the positive testing to Niagara Bottling LLC. Bratskeir also stated that Niagara has since terminated its relationship with Far Away Springs as a supplier.The expanded recall now includes 14 different name brand spring water products produced at the Allentown and Hamburg, Pennsylvania manufacturing facilities from June 10 through June 18. The recalled brand names include “Acadia Spring Water”, “Acme Spring Water”, “Big Y Spring Water”, “Best Yet Spring Water”, “7-11 Spring Water”, “Niagara Spring Water”, “Natureโs Place Spring Water”, “Preicerite Spring Water”, “Superchill Spring Water”, “Morning Fresh Spring Water”, “Shaws Spring Water”, “Shoprite Spring Water”, “Western Beef Blue Spring Water”, and “Wegmans FYFGA Spring Water”.Customers may identify the recalled bottled spring water by checking the outer wrap shrink-film or on the bottle for the affected cases with date ranges containing F# BEST BY 08Dec2016 to F# BEST BY 16 DEC2016, or A# BEST BY 08DEC2016 to A# BEST BY 16DEC2016. The F# at the beginning of the Best By dates represents the water was collected from the Hamburg plant and the A# indicates the Allentown plant.Niagara Bottling LLC claims the recalled products were shipped to Connecticut, Delaware, District of Columbia, Maine, Maryland, Massachusetts, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, Rhode Island, Vermont, Virginia, and West Virginia.For healthy individuals, E. Coli will typically cause mild to severe diarrhea and abdominal cramps, bloody stools, and sometimes minor fevers lasting between fiveย and 10 days. Individuals such as young children or the sick and elderly may be affected more because of a weakened immune system where the contamination could lead to a condition called Hemolytic Uremic Syndrome (HUS) which could lead to kidney failure and even death.Customers are being encouraged to check their bottled water to verify if it is part of the recall and to not drink the water without boiling it first kill the potential E.coli bacteria. Customers with further questions may contact Niagara bottling LLC at 877-487-7873. 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: E. Coli, Spring Water, Water ContaminationMore Lawsuit Stories Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer August 14, 2026 Whippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters August 14, 2026 Ninja Foodi Pressure Cooker Explosion Lawsuit Alleges Safety Defect Caused Severe Burns August 14, 2026 1 Comments Nichole July 10, 2015 I have purchased and drank water from shoprite that was contaminated. I was in the urgent care with extreme pains and put on antibiotics. After more testing they have found a different parasite that I need an additional medication for. My kidneys are extremely painful fr this. I have another appt on the 13th to have more tests on them to find what type of damage they have endured. 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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 Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott 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)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026) Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026) Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)
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Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott 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)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)
Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026)
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)