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.
Fleet, Other Laxatives May Cause Kidney Damage, Heart Injury, Death: FDA January 9, 2014 Irvin Jackson Add Your CommentsOverdoses of Fleet and other sodium phosphate-based laxatives can cause severe kidney damage, heart injury and even death, according to a new FDA warning. ย On January 8, the FDA issued a drug safety communication warning against the use of more than one dose or application of sodium phosphate-based laxatives, advising that too much can lead to severe and sometimes fatal side effects.The FDA indicates that taking more than one dose in 24 hours or taking more than the recommended amount of the laxatives, in either oral or enema form, can cause severe dehydration, and changes in the levels of serum electrolytes. These laxative side effects can cause damage to organs, including the heart and kidneys, potentially increasing the risk of death in some cases.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 COMPENSATIONThe warning comes after an FDA review of decades of adverse event reports and medical literature dating as far back as 1957. From that data, the FDA found dozens of cases of adults and children suffering severe health problems after overdosing Fleet and other over-the-counter sodium phosphate laxative products used to treat constipation. Most cases involved children younger than five years old and older adults.The FDA indicates that nearly half of the adult reports and two-thirds of the children involved dehydration, kidney disease, acute colitis, or delayed bowel emptying. There was also often concomitant use of drugs that affect the kidneys, such as diuretics and non-steroidal anti-inflammatory drugs (NSAIDs) like Motrin and Alleve.“All reports of serious outcomes were characterized by dehydration and/or electrolyte disturbances with associated complications such as acute kidney injury and death,” the FDA warning reports. “Nearly half of adult cases and 3% of pediatric cases reported a fatal outcome.”The FDA advises consumers to always read the Drug Facts labels and use the products as recommended, never exceeding the recommended dose. Consumers taking NSAIDs, diuretics, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers for high blood pressure, or those suffering from an inflamed colon should consult a physician before using one of these over-the-counter laxative products.The agency also warns that caregivers should never give the product to children 5 years and younger without first discussing it with a health care professional. The rectal form of the drugs should never be given to children younger than two years of age, the agency warns.Fleet Phospho-Soda Recall and LitigationThis is not the first time the FDA has warned about the risk of problems with Fleet and similar laxatives.In 2008, aย Fleet Phospho-soda recallย was issued after the FDA indicated that the over-the-counter oral sodium phosphate solution should not be used as a bowel cleanser due to the risk ofย acute phosphate nephropathy, a rare form of kidney damage.After the recall,ย more than 1,200 Fleet Phospho-soda kidney lawsuits were filed in various state and federal courts throughout the United States. Most were resolved in a global settlement in 2010.ย Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Dehydration, Fleet Phospho-soda, Kidney Injury, Laxative, Oral Sodium PhosphateMore Lawsuit Stories Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL August 24, 2026 Kratom Addiction Lawsuit Alleges Opioid-Like Products Caused Addiction, Cardiac Injury August 24, 2026 Clear Eyes Recall Issued Due to Risk Eye Drops May Be Contaminated August 24, 2026 1 Comments margaret June 29, 2014 I had fleet product renal damage may 2008 happened overnight from 100% renal function to gfr 35. I had a lawyer who told me medical paperwork came n past deadline? Can I still have recourse towards fleet. I have medical documentation proving. I had to quit work, have terrible fatigue and multiple problems medically from fleet trauma. Including original dr order to take it. Please let me kno if I can obtain responsibility from fleet now as it debilitated my health and quality of life and continues to worsen. How can there be a legal time limit when documentation, testing, worsening over time happens? What can I do? This product created hardships for me and my husband and ruined my excellent health and quality of life.. Thank you. CommentsThis 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 Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (Posted: yesterday)A federal judge has appointed a group of plaintiffs attorneys to leadership positions in the growing Boston Scientific spinal cord stimulator federal litigation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (08/18/2026)Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026) Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits (Posted: 4 days ago)Abbott Laboratories has agreed to pay $670 million to resolve more than 2,000 Similac NEC injury lawsuits, as the first federal NEC trial against competitor Mead Johnson gets underway.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITMissouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit (08/20/2026)Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week (08/11/2026)Neocate Infant Formula Lawsuit Alleges Nutritional Defect Caused Rickets, Bone Fractures (08/05/2026) Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: 5 days ago)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)
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