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.
Two Alfalfa Sprout Food Poisoning Outbreaks Tracked By CDC, FDA March 8, 2016 Russell Maas Add Your CommentsGovernment health officials are currently investigating two multi-state Salmonella and E. coli outbreaks that have been linked to alfalfa sprouts produced by two manufacturers, causing at least two dozen consumers to suffer food poisoning.ย The U.S. Centers for Disease Control and Prevention (CDC), in conjunction with the FDA, is currently reviewing at least two alfalfa sprout outbreaks that have caused illnesses with Salmonella Muenchen and E. coli O157 across six states. To date, seven have been hospitalized due to the alfalfa sprout food poisoning.The outbreaks are believed by the CDC and the FDA to be separate from one another, after trace back investigations identified alfalfa sprouts produced by Jack & The Green Sprouts of River Falls, Wisconsin was identified to be the source of the E. coli O157 outbreak and alfalfa sprouts produced by Sweetwater Farms of Inman, Kansas were pinpointed as the likely source of the Salmonella Muenchen outbreak.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 CDC is urging customers to avoid consuming alfalfa sprouts produced or distributed by the two manufacturers and to avoid consuming them if the manufacturer is unknown.Jack & Green Sprouts E. Coli OutbreakOn February 24, health officials from the Wisconsin Department of Agriculture and the Minnesota Department of Health issued a press release warning consumers to not eat alfalfa sprouts produced by Jack & The Green Sprouts after receiving nine reported illnesses of consumers who claimed to have eaten sprouts produced by the company within the week before contracting salmonella poisoning.On February 25, the FDA announced a Jack & The Green Sprouts Inc. recall of all alfalfa and alfalfa onion sprout products.Following the recall the FDA and CDC interviewed eight of the nine consumers who were suffering from the E. coli food poisoning, who reported eating alfalfa sprouts or menu items containing sprouts in the week prior to their illness. A joint effort by state, local and federal agency traceback investigations discovered that all seven of the reported locations where illnesses had occurred served alfalfa sprouts produced by Jack & The Green Sprouts Inc.Consumers and retailers are being asked to stop serving or consuming any alfalfa sprouts produced by Jack & The Green Sprouts Inc., which were packaged in a plastic clamshell container with a round, brightly colored label on the top that notes the sprout variety. Production dates of sprouts contaminated with E. coli have still not been determined.E. coli will typically causes mild to severe diarrhea and abdominal cramps, bloody stools, and sometimes minor fevers lasting between five 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.Sweetwater Farms Salmonella OutbreakSimilarly, the CDC and FDA identified the likely source of the alfalfa sprout Salmonella outbreak to sprouts produced by Sweetwater Farms through traceback investigations.On February 19, the Kansas Department of Health and Environment issued a press release warning people not to consume sprouts produced by Sweetwater Farms after thirteen people from Kansas (5), Missouri (3), Oklahoma (3), and Pennsylvania (2) became ill with Salmonella Muenchen poisoning.The CDC and FDAโs interviews with sickened consumers indicated 10 or the 12 people reported eating sprouts from grocery stores or restaurants the week before suffering salmonella food poisoning. Nine of the 10 individuals specifically reported eating alfalfa sprouts. State and local health and regulatory officials performed traceback investigations that discovered the five locations where sickened consumers had eaten all were supplied alfalfa sprouts by Sweetwater Farms.According to the CDC, recent lab tests isolated salmonella from samples of irrigation water collected at Sweetwater Farms during a routine inspection. These strains are being tested to see if they caused the current outbreak.Salmonella infections can cause mild to severe health consequences, depending upon the individual. The bacteria may cause a healthy person to experience fever, diarrhea, nausea, vomiting, and abdominal pain, whereas the young or elderly with weakened immune systems may face more severe consequences, including fatal infections.In some reported cases, Salmonella infections in pregnant women have been known to cause still births and miscarriages. Occasionally, salmonella infections may travel through the bloodstream and produce illnesses such as arterial infections, endocarditis and arthritis.Both the CDC and FDA are asking customers to avoid eating sprouts produced by Sweetwater Farms and Jack & The Green Sprouts until the investigation can determine the extent of the potentially contaminated sprouts. Illnesses from those who became sick after early February may not be reported yet, due to the average two to four weeks it takes for a consumer to report their illness. 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: Alfalfa Sprout, Alfalfa Sprout Recall, E. Coli, Food Poisoning, SalmonellaMore Lawsuit Stories Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial October 6, 2026 Lawsuit Alleges FreeStyle Libre 3 Plus, iLet Insulin Pump Device Failures Caused Death October 6, 2026 Uber Sexual Assault Settlement Reached Before Bellwether Trial Begins October 6, 2026 0 Comments FacebookThis 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 Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial (Posted: today)A federal judge has selected the third claim to serve as a Covidien hernia mesh bellwether trial, which will begin in March.MORE ABOUT: HERNIA MESH LAWSUITJudge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (09/11/2026)Covidien 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) Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: yesterday)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026) Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 4 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)
Lawsuit Alleges FreeStyle Libre 3 Plus, iLet Insulin Pump Device Failures Caused Death October 6, 2026
Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial (Posted: today)A federal judge has selected the third claim to serve as a Covidien hernia mesh bellwether trial, which will begin in March.MORE ABOUT: HERNIA MESH LAWSUITJudge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (09/11/2026)Covidien 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)
Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: yesterday)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)
Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 4 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)