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.
FAA Safety Oversight To Get Overhaul Following Concerns Over Boeing 737 MAX Certification: Report March 27, 2019 Martha Garcia Add Your CommentsFederal aviation regulators indicate that two recent accidents involving the now-grounded Boeing 737 MAX passenger airplane are signs that an update is needed to the nation’s air safety oversight.According to a report by Reuters, U.S. Transportation Department Inspector General, Calvin Scovel will testify today before the U.S. Senate Commerce Committee and is expected to indicate that the U.S. Federal Aviation Administration (FAA) will make significant changes to itโs safety inspection process for passenger jets.The promise comes after a fallout from what is largely viewed as a regulatory failure that may have resulted in two high-profile crashes involving the 737 MAX, which killed more than 300 people.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 COMPENSATIONOn October 29, 2018, Lion Air Flight 610 crashed into the sea just 13 minutes into its flight, killing all 189 passengers and crew. Black box and flight data recorders indicate the pilots fought for 11 minutes to keep the plane in the air,ย likely due to a problem with the planeโs Angle of Attack (AOA) sensor, which kept telling an automated system, which the pilots could not shut off, to point the nose down.On March 10,ย Ethiopian Airlines Flight 302 crashed just minutes into its flight, killing all 157 passengers and crew. And investigators in both France and the FAA are saying that the characteristics of the short flight look disturbingly similar to that of the ill-fated Lion Air flight.The two crashes have raised questions about what Boeing and the FAA knew about potential problems with the Boeing 737 Max, as other reports of averted accidents have surfaced in recent weeks.The two crashes resulted in the grounding of the Boeing jet worldwide. Most countries began grounding the jets soon after the second crash. China, the European Union, and Canada were among the first countries to take the safety step and ground their entire fleets. On March 14, the U.S. was the last major country to ground the planes.Todayโs hearing focuses on the safety of the jets and the FAAโs response and involvement. The ongoing investigation into the accident has revealed that the agency gave Boeing significant leeway in policing itself and critics have raised questions over how long it took the FAA to ground the planes.Despite the 737s being made in the United States. Ethiopian officials asked French investigators to examine the recovered black box and flight data recorders from the most recent crash, saying they did not trust the FAA.Boeingโs 737 MAX planes are manufactured in the U.S., the Trump administration heavily promoted sales of the planes throughout the world, and early indications suggest the FAA let Boeing do much of its own safety oversight.Acting FAA Administrator Dan Elwell has said the agencyโs safety culture โmust evolve.โ As a result, the FAA has agreed to improve oversight of organizations performing jet inspections on their behalf. The agency reportedly plans to implement the new oversight approach by July.Crash Investigations OngoingThe Department of Transportation and the Federal Bureau of Investigation have launched a criminal probe into the certification of the Boeing 737 MAX jet, in addition to ongoing investigations by the National Transportation Safety Board as well as French investigators who are examining the Ethiopian Airlines flightโs black box.The FAA says the 737 MAX will return to service when the agencyโs analysis of safety data indicates it is appropriate.Boeing submitted an anti-stall software upgrade to the FAA on January 21. The upgrades are intended to prevent repeated operation of the anti-stall system and will deactivate it if it receives conflicting sensor information. In the Lion Air accident, pilots were unable to deactivate automated systems which kept trying to point the nose of the plane down to prevent a stall. Initial analysis of the Ethiopian Airlines crash suggests there may have been a similar problem.Some reports revealed the override for the automated system was sold at an additional cost to customers as an optional upgrade. Boeing indicates it will now make the warning light standard.The FAA has tested the upgrade in simulator and aircraft situations. However, the agency plans to release more information about the upgrade in the coming weeks.The 737 MAX is Boeingโs best selling aircraft with $500 billion at list prices. The company had 400 planes in operation around the world with orders for 5,000 more before countries began grounding the jets after the recent crashes. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Airplane, Airplane Accident, Boeing, Congress, FAAMore Lawsuit Stories Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks October 1, 2026 Amazon Coowalk Heated Insoles Lawsuit Alleges Lithium-Ion Battery Explosion Caused Severe Burns October 1, 2026 Chlorpyrifos Ban Takes Effect Across EU as Studies Link Pesticide Exposure to Parkinsonโs Disease October 1, 2026 0 Comments InstagramThis 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 Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: yesterday)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026) Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: yesterday)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026) Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (Posted: 3 days ago)A Texas woman’s Boston Scientific SCS implant lawsuit claims she spent several years with a broken device in her back, but did not remove it because the company’s sales representatives said it just needed reprogramming.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (09/10/2026)
Amazon Coowalk Heated Insoles Lawsuit Alleges Lithium-Ion Battery Explosion Caused Severe Burns October 1, 2026
Chlorpyrifos Ban Takes Effect Across EU as Studies Link Pesticide Exposure to Parkinsonโs Disease October 1, 2026
Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: yesterday)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026)
Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: yesterday)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)
Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (Posted: 3 days ago)A Texas woman’s Boston Scientific SCS implant lawsuit claims she spent several years with a broken device in her back, but did not remove it because the company’s sales representatives said it just needed reprogramming.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (09/10/2026)