MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking
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.
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
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.
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.
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.
Hummus Recall Issued Again by Sabra Over Listeria Risks November 21, 2016 Russell Maas Add Your CommentsCertain Sabra hummus products have been recalled, after testing confirmed the presence of listeria monocytogenes thatย may cause serious and sometimes fatal infections, particularly among young children, the elderly and those with weakened immune systems.ย The FDA posted the Sabra hummus recall on November 19, after listeria was found on equipment at a Virginia manufacturing facility during routine testing. To date, investigators have not found any listeria in products that made it to shelves, and no listeria food poisoning incidents have been linked to the recalled hummas.Sabra Dipping Co. announced on the recall on their Twitter account on Saturday, adding that the company has halted production to thoroughly clean and sanitize the entire plant where the listeria was found.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 COMPENSATIONIncluded in the recall are various flavors and sizes of hummus products manufactured prior to November 8, 2016. Sabra is recalling all hummus products with a โBest Beforeโ date up through January 23, 2017. Customers are being asked to stop consuming the products immediately and confirm the โBest Beforeโ date on the lid of the package. Sabra Organic Hummus, Sabra Salsa, Sabra Guacamole and Sabra Greek Yogurts are not included in the recall.For a full list of the recalled products and UPC codes please visit the FDA recall notice linked above.This is the second time in two years that a Sabra recalled hummus due to listeria risks. A Sabra Classic Hummus recall, affecting bout 30,000 cases, was announcedย in April 2015, after random sample testing by Michigan inspectors found the presence of listeria. No illnesses were reported in connection with that recall either.Listerosis is a foodborne illness that can cause serious health consequences and death, especially for children, the elderly and those with weakened immune systems. The infection is considered by the FDA as one of the more dangerous foodborne illnesses and frequently results in hospitalizations and carries a 25% fatality rate.Symptoms of listeria infections may include nausea, muscle ache, diarrhea, fever, and fatigue. In severe cases for the elderly and young children, the bacteria could spread through the bloodstream to the nervous system resulting in sometimes fatal infections. For pregnant women, listerosis can pose a risk of miscarriages, still births, premature delivery or life-threatening infection of the newborn.Customers with recalled hummus products are being asked to discard them or to visit the manufacturer online at www.sabrahummusrecall.com for a reimbursement. Customers with further questions regarding the recall may contact Sabra Consumer Relations at 1-866-265-6761. 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: Hummus Recall, Listeria, Listeria Food Poisoning, SabraMore Lawsuit Stories MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026 Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026 Lawsuit Claims Werner Stepladder Collapsed, Leaving Woman With Skull Fracture and Brain Injury August 12, 2026 0 Comments X/TwitterThis 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 CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL 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)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 5 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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