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.
Kugel Hernia Patch Manufacturer Cited for Violations at Puerto Rico Plant October 15, 2008 AboutLawsuits Add Your CommentsThe FDA released a warning letter yesterday that was sent to C.R. Bard, Inc. regarding “adulterated” medical products manufactured at their plant in Puerto Rico, which is where the company manufactures the Kugel Hernia Patch mesh that has been the subject of thousands of lawsuits in the United States.Inspections at the plant between November 20, 2007 and February 13, 2008, revealed a number of violations of Good Manufacturing Practice requirements of federal regulations.The company was warned about a number of problems, such as failing to make sure that products made conform to their design requirements, failing to identify products with quality issues and other violations which could raise questions about the safety of medical products made at the plant.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 FDA letter, which was dated July 22, 2008, also indicates that C.R. Bard received a number of consumer complaints during 2006 and 2007 involving mix-ups and mislabeled products. In one case, the FDA states that Bard sold “Bard Modified Kugel Patch” products labeled both on the box and the sterilized pack as medium, even though they were the small size.“We are very concerned by your continual practice of failing to extend investigations and corrective actions to your distributed products,” wrote Maridalia Torres, the FDA San Juan District Director in the letter sent to John Weiland, the President and CEO of C.R. Bard, Inc.C.R. Bard has issued three separate Kugel Hernia Patch recalls since 2005, even though there is no indication that the violations cited in the warning letter have anything to do with the design defects that prompted the recalls.Bard also faces over 2,000 Kugel Hernia Patch lawsuits filed by patients who suffered serious internal injuries after hernia surgery, such as bowel perforations, chronic intestinal fistula and death.The Bard plant in Humacao, Puerto Rico was constructed in 2003. According to the company’s website, they manufacture a variety of products at the plant, including Davol hernia mesh products like the Kugel patch; grafts, fabrics, shunts and the Vacora Biopsy System for Bard Peripheral Vascular; catheters and feeding devices for Bard Access Systems, and Tegress T bulking agent for Bard Urological Division. Tags: Bard, Davol, Hernia, Kugel, Mesh, PatchMore Lawsuit Stories DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data June 26, 2026 Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial June 26, 2026 Study Finds Dose Response Link Between Alcohol and Pancreatic Cancer June 26, 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 DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data (Posted: 2 days ago)A proposed class action lawsuit alleges DraftKings secretly shared website visitors’ personal information with third-party data brokers to build consumer profiles without their consent. Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (Posted: 3 days ago)A federal judge has scheduled the first Dupixent lawsuit MDL initial case management conference for October 1, 2026.MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock 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) Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: 4 days ago)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)
Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial June 26, 2026
DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data (Posted: 2 days ago)A proposed class action lawsuit alleges DraftKings secretly shared website visitors’ personal information with third-party data brokers to build consumer profiles without their consent.
Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (Posted: 3 days ago)A federal judge has scheduled the first Dupixent lawsuit MDL initial case management conference for October 1, 2026.MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock 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)
Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: 4 days ago)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)