Chesapeake Regional Lawsuits Filed by Nearly 1,000 Women Who May Have Undergone Unnecessary Surgeries
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.
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.
AngioDynamics Port Catheter 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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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.
Bausch and Lomb PreserVision Eye Vitamin Recall: Choking Hazard July 29, 2010 Staff Writers Add Your Comments Bausch and Lomb’s PreserVision Eye Vitamin soft gel pills are being recalled because they have been found to be difficult for some consumers to swallow safely, which could cause a chocking sensation, particularly among the older consumers. The PreserVision eye vitamin recall was announced on Tuesday by the FDA and Bausch and Lomb. The manufacturer has received several reports indicating some users were feeling like they were choking after having difficulty swallowing. Most of the reports came from people 70 or older, the company said. The recall is limited to the PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 soft gels, which is only available in the United States. Bausch and Lomb says that the formulation is safe and that most customers have no problem swallowing the pills, but the difficulties experienced by elderly consumers has made them reconsider the soft gel design used in the pill. Do You Know about… SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The affected pills are sold in 60-count bottles and are taken twice per day, two pills per dose. The recalled vitamins have a UPC code of 24208 62584, and have the following lot numbers: 0923BK103, 0924BK103, 0924BK103A, 0925BK103A, 0926BK103A, 0927BK103A, 0928BK103A, 0929BK103A, and 0930BK103A. The pills have an expiration date of 8/31/2011. Both U.S. retailers and eye care professionals have been alerted regarding the recall. Bausch and Lomb recommends anyone who has the recalled eye vitamins return the product to the company for reimbursement, even if they are comfortable swallowing the pills. The company’s customer service number is 1-800-553-5340. Tags: Bausch and Lomb, Drug Recall, PreserVision Eye Vitamin More Lawsuit Stories Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks March 10, 2026 Uber Sexual Assault MDL Judge Considered Expanding Jury Pool in Next Bellwether Trial March 10, 2026 Chesapeake Regional Lawsuits Filed by Nearly 1,000 Women Who May Have Undergone Unnecessary Surgeries March 10, 2026 3 Comments Linda December 12, 2023 I have used preservision areds2 for over a year. The bottle I just opened the pills are sticky and orange to reddish color on the plastic inside the bottle.,, No one will mention if they are still ok to use.. l I have 2 bottles of 210 gels in each. one box has not been opened and does seem to rattle nicely so maybe that is not affected…l what to do, I used a coupon but still expensive. Michael May 29, 2022 I, too, I am having difficulty swallowing these caplets, even when taken with food. The bulbous shape of the caplet and it’s rather large size cause it to get stuck in the esophagus. The outer coating material also breaks down very slowly (put one in a glass of water and you will see that it doesn’t break down at all!) and no amount of saliva helps to get these caplets dislodged. B&L should definitely be made aware of how many people are having this problem. A good class action lawsuit might wake them up. STEVEN May 12, 2022 i have been on Preservision red tablets for two years and I am beginning to have extreme choking problems in trying to swallow the tablet.. They are in my onion dangerous in hat regard. I am a family physician and member of f the American Academy of Family Physicians. There should be a warning label on the tablets 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. 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Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks March 10, 2026
Chesapeake Regional Lawsuits Filed by Nearly 1,000 Women Who May Have Undergone Unnecessary Surgeries March 10, 2026
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)
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Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (Posted: 4 days ago) In a joint statement, plaintiffs and defendants in AngioDynamics port catheter lawsuits have laid guidelines for what types of cases should be selected to serve as potential bellwether trials. MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Blood Clot Results in Lawsuit Against Device Manufacturer (02/04/2026)SmartPort Infection Lawsuit Alleges AngioDynamics Catheter Defects Forced Surgical Removal (01/30/2026)Severe Sepsis Infection Leads to Vortex Port Catheter Wrongful Death Lawsuit (01/12/2026)