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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
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 Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss May 21, 2026 Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026 Lawsuit Alleges Boston Scientific Urinary Sphincter Failed, Required Additional Surgery May 21, 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 Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: today)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimer’s Disease Risks Questioned in New Study (04/27/2026) Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: yesterday)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone ‘Schedule A’ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026) Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: 2 days ago)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)
Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026
Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: today)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimer’s Disease Risks Questioned in New Study (04/27/2026)
Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: yesterday)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone ‘Schedule A’ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: 2 days ago)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)