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.
Meat and Poultry Parasite Control Rules May Be Streamlined by USDA March 23, 2016 Martha Garcia Add Your CommentsFederal food regulators plan to streamline and consolidate rules designed to prevent Trichinella and other parasites in pork and other meat products.The U.S. Department of Agriculture’s (USDA) Food Safety and Inspection Service (FSIS) issued proposed rule changes on March 18, which would eliminate redundant controls for Trichinella prevention, as a supplement to a 2001 FSIS ruling that proposed food safety standards for all ready-to-eat and all partially heat-treated meat and poultry products.The guidelines remove provisions for the prescribed treatment of pork products. However, food producers would still be required to control for the risk of Trichinella by developing and establishing science-based controls. The changes also consolidate regulations for thermally processed and commercially sterile pork meat, including canned meat.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 the FSIS, the change clarifies regulatory requirements and eliminates redundant equipment descriptions, whileย updating wording to reflect FSIS organizational structure and clarifying regulatory requirements.Trichinella spiralis is a roundworm parasite that infects both humans and animals, but swine is the primary source of infected meat ingested by humans. Humans can become sick with Trichinella by eating infected meat or by consuming raw or under cooked meat products.Nearly 400 cases were recorded each year on average since 1940, but the incidence of Trichinella has decreased to only sporadic outbreaks over past 20 years. Most of the headway was gained by improving swine raising practices.Symptoms of Trichinella food poisoning typically begin two weeks after eating tainted pork and can last up to eight weeks. Symptoms include muscle pain, fever, swelling of the face, eyes weakness or fatigue, headache, chills, itchy skin or rash, cough, diarrhea, and constipation.Infection Risk Higher Among Pasture-Raised PigsThe risk of Trichinella is higher among organic pasture-raised animals that have access to rodents and wildlife infected with the parasite. Pasture raising has increased as customer demand has increased.โRaising swine outdoors poses major risk for swine being infected with Trichinella because it increases exposure to potentially infected reservoir hosts,โ according to the FSIS.The FSIS released a compliance guide which outlined best practices focusing on the changes and highlighting the guidelines designed to help small and very small establishments to easily follow the rules.The guidelines focus on ways to reduce the incidence of Trichinella poisoning and other parasites by employing swine production practices that eliminate the sources of exposure to this parasitic hazard. Those include getting pork from producers who participate in negligible risk compartment and certification programs that reduce the incidence.Other prevention techniques include focusing on rodent and wildlife control programs to prevent swine exposure to infected wildlife, ensuring the integrity of swine feed sources and storage areas, insuring raw food waste is not fed to pigs, practicing good management and hygiene, and preventing cannibalism among the swine.Controlling Trichinella can also be done after the swine has been slaughtered for meat by heating, freezing, curing, and exposing pork products to high pressure processing and irradiation.The FSISย is asking for public comment on the proposed guidelines. The public comment period will be open for 60 days from the date the guidelines were announced. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Infection, Pork, TrichinellaMore Lawsuit Stories Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 September 11, 2026 DraftKings Lawsuit Indicates ‘Event Contracts’ Are Nothing More Than Sports Bets September 11, 2026 Social Media Wrongful Death Lawsuit Links Major Platforms to Child Suicides September 11, 2026 0 Comments PhoneThis 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 Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 2 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 3 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 4 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard 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)
Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 2 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 3 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 4 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard 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)