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.
Graco Recalls 5M Strollers Due to Amputation Risk November 21, 2014 Russell Maas Add Your CommentsNearly 5 million Graco and Century-branded strollers are being recalled, following reports of children getting their fingers amputated in the folding hinges at the sides of the strollers, which pose a pinch and laceration hazard.ย The Graco stroller recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on November 20, following at least 11 consumer reports involving finger injuries suffered by children, including at least six incidents where the fingertip was amputated, four reports of partial-fingertip amputation and one finger laceration.The recalled strollers pose a laceration and amputation hazard to children, due to the reachable sliding fold-lock hinge on each side of the stroller. Children may be able to place their fingers and hands into the side of the stroller where the sliding hinge is placed, potentially allowing them to engage the locking mechanism with their fingers inside of the hinge.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 COMPENSATIONEleven different models of Graco and Century strollers are included in the recall, which impacts roughly 4.7 million strollers sold throughout the United States, about 202,000 in Canada, and an estimated 10,300 in Mexico.The models were sold under the brand names Aspen, Breeze, Capri, Cirrus, Glider, Kite, LiteRider, Sierra, Solara, Sterling and TravelMate Model Strollers and Travel Systems.All recalled models are single-occupant strollers, with an external sliding fold-lock hinge on each side and a one-hand fold release mechanism on the handle. The impacted strollers have manufacture dates ranging from August 1, 2000 to September 25, 2014 and have the model numbers and date of manufacture printed on a white label located at the bottom of the stroller leg. For a full list of recalled models and model numbers please visit the CPSC recall announcement.The strollers were manufactured in China under Graco Childrenโs Products, of Atlanta, Georgia where they were sold at Target, Toys R Us, Walmart and other retail stores nationwide and online at Amazon.com Walmart.com, and other various online retailers from August 200 through November 2014 for between $40 and $70 for the strollers and about $140 to $170 for the Travel System.Other Major Stroller Problems This YearThe massive recall is at least the second major problem linked to Graco strollers this year. In June, several models of Graco strollers including the Ready2Grow Classic Connect strollers were placed on the CPSCโs โDonโt Buy: Safety Riskโ list, due to a possible roll-away hazard.The CPSC evaluated the strollers’ braking mechanisms to test the durability and strength claiming that the strollers plastic teeth braking mechanism is not sufficient. The agency tested the strollers by loading the seat of the Ready2Grow Classic Connect stroller with 35-40 pounds and placing the stroller on an 18 degree incline, where it began to slowly give and start rolling away. Upon evaluating the braking mechanism, the agency noticed the plastic teeth designed to lock the strollers brakes in had shown stress marks, leading to the agency questioning the vulnerability and durability of the devices.Additionally, this is the second recall this year of strollers that carry an amputation risk. In late January 2014, the CPSCย announced a Britax stroller recall that impactedย roughly 224,000 baby strollers, following reports of the strollers snapping down on customerโs hands, including one report of a partial finger amputation and one incident involving a broken finger with severe lacerations. After receiving the injury reports, an investigation by the CPSC and Britax noticed a risk of problems that may occur when the release button is pressed while pulling on the release strap. When this happens, the stroller may pinch the userโs finger, posing a laceration and amputation hazard.Due to an influx in infant stroller accidents and injury reports in recent years, the CPSC passed new stroller safety standards on March 4, which will add new requirements to how all strollers and carriages will be made, tested, and labeled.The new requirements will impact all strollers sold after September 2015, addressing potential risks with head entrapments associated with adjustable grab bars, broken wheels, parking break failures, locking mechanism problems, restraint issues, structural integrity and stability, and hinge issues that have been known to cause pinching and amputations of fingers like those of the latest recall.Graco is asking to consumers to contact them immediately for a free repair kit at 800-345-4109 or by visiting them online at www.gracobaby.com and navigating to the โHelp Centerโ.Free Graco recall repair kits will be available in early December 2014. Until then consumers have been urged to exercise extreme care when folding the stroller and to be sure that the hinges lock before placing the children in the stroller. Caregivers should remove children from the strollers immediately if the hinges begin to fold after the hinges have been locked to prevent laceration and amputation hazards. 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: Amuptation, Baby Stroller Recall, Graco, Graco StrollerMore Lawsuit Stories Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026 Omnipod Class Action Lawsuit Filed Over Recalled Insulin Delivery System July 7, 2026 Lack of Safety Features Led to Roblox Child Exploitation, Lawsuit Claims July 7, 2026 0 Comments CompanyThis 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 Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026) Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration (Posted: yesterday)A Texas man’s lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026) Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (Posted: 5 days ago)Federal warnings and enforcement actions involving Olympus and other reusable medical scopes have raised concerns that design flaws may allow bacteria to remain trapped after cleaning, leading to serious infections and product liability lawsuits.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026
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