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.
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
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.
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.
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.
Solar Eclipse Glasses Recall Suggests Certain Products May Not Be Safe August 14, 2017 Russell Maas Add Your CommentsWith a total solar eclipse visible within a band across the entire United States next week, millions of Americans have purchased safety glasses to protect their eyes while viewing the rare event. However, it appears that certain solar eclipse glasses sold by Amazon do not comply with industry standards, and may pose a risk of eye injury or vision impairment if used.Amazon announced the solar eclipse glasses recalls in e-mails sent to customers on August 12, indicating that there were safety concerns involving several brands that may not provide adequate UV ray protection when viewing the total solar eclipse on August 21, 2017.The recall was issued after Amazon recognized the manufacturers of the solar eclipse glasses distributed on their site were not among those recommended by NASA or the American Astronomical Society (AAS), and could potentially harm customers when viewing the solar eclipse event. The recalls were announced out of an abundance of caution, according to a statement provided to customers that previously purchased the two brands of recall solar eclipse glasses.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 recalled solar eclipse glasses includes various brands, such as Agena Astro brands from Los Angeles, California and Lunt Solar System brands of Tucson, Arizona, among a few others, which may not have provided sufficient evidence that their products meet the requirements, specifications, guidelines or characteristics set forth by the International Organization for Standardization (ISO).Owner of Agena Astro Products released a statement on Amazons website claiming his glasses, which have been the best seller for the last month, are appropriately designed for safe viewing of the total solar eclipse, and that the products are currently being submitted to NASA for safety verification.Solar eclipse glasses have been one of the most popular items on Amazon over the last month, as people prepare for the total solar eclipse that will occur on Monday, August 21, 2017.A total solar eclipse is an event in which the moon passes directly in front of the sun, completely blocking the sun along the 70-mile-wide corridor stretching from Oregon all the way across the United States to South Carolina.According to the AAS, individuals planning on viewing the event are encouraged to never look directly into the sun without proper, approved eye protection to avoid serious injuries such as eye irritation or blindness.As a safety measure, the solar eclipse glasses not included on the AAS recommended manufacturers list should not be for viewing the total solar eclipse event. A list of the recommended manufacturers can be found on the AAS website at https://eclipse.aas.org/resources/solar-filters.Customers who are in possession of recalled solar eclipse glasses purchased through Amazon.com, will be awarded a refund within seven to ten business days and are being asked to not use the solar eclipse glasses for the event. 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: AmazonMore Lawsuit Stories Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 September 14, 2026 Colsen Tabletop Fire Pit Lawsuit Alleges Defective Design Caused Flame Jetting Burn Injuries September 14, 2026 Roblox Arbitration Clause Opposed by U.S. Senators in Child Sexual Assault Lawsuit Appeal September 14, 2026 0 Comments EmailThis 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 Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (Posted: today)Attorneys will meet tomorrow for a final pretrial conference ahead of the third Bard PowerPort lawsuit bellwether trial.MORE ABOUT: BARD POWERPORT LAWSUITJury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026) Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 3 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 4 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
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Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (Posted: today)Attorneys will meet tomorrow for a final pretrial conference ahead of the third Bard PowerPort lawsuit bellwether trial.MORE ABOUT: BARD POWERPORT LAWSUITJury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)
Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 3 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 4 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)