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.
Velvet Ice Cream and Sherbet Products Recalled Due to Listeria Risk April 29, 2021 Irvin Jackson Add Your CommentsA recall has been issued for dozens of different brands of ice cream and sherbet, which were sold under names like Velvet, North Star, Super Dip and others, due to a risk of listeria food poisoning.The FDA announced the ice cream recall on April 27, ย after the manufacturer revealed the products may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.Velvet Ice Cream, the manufacturer, discovered listeria contamination during routine company testing and then informed the FDA of the problem. Although the bacteria poses serious health risks, there are no confirmed illnesses or injuries reported in connection with the recalled ice cream and sherbet products.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 recall impacts more than 90 different products of Velvet ice cream and sherbet, which were sold under the Velvet brand name, as well as the Buehlerโs, Discount Drug Mart, North Star, Whale of a Pail, and Super Dip brand names. A full list of affected products is available in the recall announcement.The ice cream and sherbet products were made on or since March 24, 2021, and were distributed throughout Kentucky, Indiana, Ohio, and West Virginia through convenience stores and supermarkets with varying sizes and containers.โWeโre conducting this voluntary recall in cooperation with the FDA out of consideration for the wellbeing and safety of our customers and consumers,โ said Velvet Ice Cream CEO Luconda Dager. โWe continue to be committed to serving consumers with high quality ice cream and sherbet products.โThe Listeria monocytogenes organism can cause serious and sometimes fatal infections in young children, frail or elderly people, posing a particularly serious risk for persons with weakened immune systems. However, even healthy individuals can suffer side effects, including short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Among pregnant women, listeria monocytogenes infections can cause miscarriages and stillbirths.Listeria poisoning symptoms usually start one to four weeks after eating food contaminated with the bacteria, but can start the same day or even up to 70 days after consumption. In some cases, severe illness may result if the bacteria spreads beyond the gut to other areas of the body. The U.S. Centers for Disease Control and Prevention (CDC) advise speaking with a doctor if you experience any symptoms of headaches, stiff neck, confusion, loss of balance, convulsions, fever and muscle aches after eating the contaminated product.The FDA and Velvet Ice Cream recommend consumers throw away or return any recalled products to the store of purchase for a full refund. Customers with questions may contact Velvet Ice Cream at 800-589-5000, extension 237, or by visiting the companyโs website at http://www.velveticecream.com/contact-us. 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: Ice Cream Recall, Listeria, Listeria Food PoisoningMore Lawsuit Stories Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot June 18, 2026 Nexgrill Class Action Lawsuit Alleges Manufacturer Botched Grill Brush Recall June 18, 2026 RAEV E-Bike Lawsuit Claims Battery Fire Caused $1.6M in Property Damage June 18, 2026 0 Comments NameThis 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 Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: yesterday)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026) Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: 2 days ago)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026) Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: 3 days ago)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)
Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot June 18, 2026
Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: yesterday)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)
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Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: 3 days ago)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)