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.
Trek Bike Recall Issued Following Reports of Severe Injury, Including Quadraplegia April 23, 2015 Russell Maas Add Your CommentsFollowing several reports of serious injuries associated with certain Trek bicycles, including one rider who suffered a fracture and another who is now a quadriplegic, almost 1 million bikes equipped with front disc brakes are being removed from the market.The Trek bike recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on April 21, after the company realized that the front wheel quick release lever may loosen and come into contact the front disc brake assembly, causing the front wheel to come to a sudden stop and potentially separate from the bike. This poses a serious risk of bike crashes and falls for the rider.At least three reports of problems with the Trek bike wheel release are known to have resulted in accidents, including one rider who experienced facial injuries from falling, another who suffered a broken wrist upon impact with the ground, and another third rider who suffered catastrophic injuries resulting in paralyzation of all four limbs due to a spinal cord injury.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 includes all models of Trek bicycles from 2000 through 2015 that are equipped with front disc brakes and a black or silver quick release lever located on the front wheel hub. Owners may identify if their bicycles are included in the recall and verify riding safety by opening the quick release lever all the way. If the release lever opens to a full 180 degrees from the closed position and it is contacting the disc brakes, the bike is included in the recall.An estimated 900,000 of the recalled bicycles were sold in the United States, with another 98,000 distributed for sale in Canada.The recalled Trek bikes were manufactured in Twain and China, whereas the quick release was only manufactured in Taiwan. Both were imported by Trek Bicycles Corporation of Waterloo, Wisconsin where they were sold at bicycle stores nationwide from about September 1999 through April 2015 for between $480 and $1,560.The CPSC recommends that customers with recalled Trek bicycles stop using them immediately and contact an authorized Trek retailer for a free installation of a new quick release on the front wheel. Customers will be given a $20 coupon that is redeemable by December 31, 2015 toward any Bontrager merchandise. Owners with further questions may contact Trek Bicycle Corporation at 800-373-4594 or visit them online at www.trekbikes.com. 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: Bicycle Accident, Bicycle Recall, Personal Injury, Trek Bicycle RecallMore Lawsuit Stories Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway October 14, 2026 Lawsuit Alleges Apple AirTag Tracker Used to Monitor Womanโs Location October 14, 2026 Heart Valve Lawsuit Alleges Abbott Trifecta GT Failed Years Earlier Than Expected October 14, 2026 0 Comments 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 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 Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: today)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026) GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (Posted: yesterday)A Florida manโs lawsuit claims he became legally blind after developing NAION while using the diabetes drug Ozempic.MORE ABOUT: OZEMPIC LAWSUITOzempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (09/08/2026) Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (Posted: 2 days ago)Boston Scientific SCS implant litigation is moving toward a process that will speed up future lawsuit filings as the number of claims continues to rise.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)
Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: today)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)
GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (Posted: yesterday)A Florida manโs lawsuit claims he became legally blind after developing NAION while using the diabetes drug Ozempic.MORE ABOUT: OZEMPIC LAWSUITOzempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (09/08/2026)
Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (Posted: 2 days ago)Boston Scientific SCS implant litigation is moving toward a process that will speed up future lawsuit filings as the number of claims continues to rise.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)