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.
Chlorpyrifos Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
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.
Listeria Outbreak Leads to “Soft Serve On The Go” Ice Cream Cup RecallInvestigators found bacterial contamination in a “Soft Serve” ice cream cups purchased by an individual who was hospitalized with listeria food poisoning. August 11, 2023 Katherine McDaniel Add Your CommentsFederal investigators have announced a recall of Real Kosher soft serve ice cream cups following at least two reports of listeria food poisoning.The U.S. Centers for Disease Control and Prevention (CDC) issued the listeria food poisoning outbreak alert on August 10, linking illnesses in New York and Pennsylvania with a Real Kosher Ice Cream “Soft Serve on the Go Cups” recall announced by the Food and Drug Administration (FDA) on August 9.The CDC launched an investigation into the products after listeria bacteria was found in an ice cream cup purchased by one of the food poisoning victims. The agency is now conducting further tests to determine if it is the same strain that has been causing the listeria outbreak.Listeria is a dangerous and sometimes fatal foodborne illness that may cause serious health complications in those with weakened immune systems, such as children, pregnant women and the elderly.Real Kosher Ice Cream RecallThe Real Kosher Ice Cream recall impacts all flavors of “Soft Serve on The Go” ice cream and sorbet cups produced on or before August 4, 2023. The products were distributed in grocery and convenience stores, schools, camps, nursing homes, and long-term health care facilities in 20 different states.According to the recall notice, the products were packaged in a sealed clear plastic container and came with an attached spoon. Consumers may identify the recalled products using the UPC code printed on the package, however, the ice cream cups were not labeled with a lot number or best by date.The recall includes the following Soft Serve on the Go cups flavors and UPC codes:Vanilla Chocolate: UPC 0-91404-15129-0Razzle: UPC 0-91404-15133-7Caramel: UPC 0-91404-15131-3Parve Vanilla Chocolate: UPC 0-91404-15113-9Sorbet Strawberry Mango: UPC0-91404-15128-3Lite Peanut Butter: UPC0-91404-15285-3Real Kosher Ice Cream has halted production and distribution of the products until federal health officials’ conclude their investigation and determine the source of the listeria contamination.The CDC and FDA advise consumers and distributors to check their freezers for products that may be affected by the recall, and immediately dispose of them, or return them to their original place of purchase to receive a refund.For more information, consumers may contact Real Kosher Ice Cream’s customer service by calling 845-668-4346, or emailing info@softserveonthego.com, Monday through Friday from 9 am to 5 pm EST.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 COMPENSATIONListeria Food Poisoning RisksOfficials warn the number of food poisoning illnesses linked to the soft serve ice cream cup listeria outbreak may be higher than currently reported, as healthy individuals normally recover without requiring medical treatment, and infection symptoms may not appear until days or weeks after exposure to the harmful bacteria. In addition, health officials indicate that listeria bacteria in the contaminated ice cream cups may survive temperatures below freezing, posing a continuing risk if the products are not removed from inventory.While healthy individuals usually experience mild symptoms, including fever, headache, nausea, stiffness and diarrhea, listeria infections can cause serious health consequences for vulnerable individuals. The bacteria in Real Kosher Ice Cream cups pose a particular concern, since the products were widely distributed in hospitals, nursing homes and long-term care facilities, where individuals with compromised immune systems may be served the products.Listeria infection symptoms normally occur within 2 weeks of exposure, but can start as early as the same day, or appear as late as 10 weeks after. The infection can spread to other parts of the body and lead to severe health conditions in vulnerable individuals that may require hospitalization or result in death, and pregnant women may experience miscarriage, premature birth, or spread life-threatening infections to their babies.The listeria outbreak investigation is still ongoing, and federal health regulators will issue additional guidance as more information becomes available.For more information on the listeria outbreak, the CDC recommends consumers visit their Listeria Questions and Answers page, or contact their state’s health department with questions. Tags: Ice Cream Recall, Listeria, Listeria Food Poisoning, New York, PennsylvaniaMore Lawsuit Stories Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026 Indoor Fire Pit Lawsuit Indicates Flame Jet Set User’s Body on Fire August 20, 2026 Missouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit August 20, 2026 0 Comments 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 Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: today)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) FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: yesterday)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro 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)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026
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Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro 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)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)