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.
Qbit Stroller Recall Due to Risk of Sudden Closing, and Laceration Risk from Hinge Mechanism December 21, 2016 Russell Maas Add Your CommentsNearly 30,000 Qbit infant and child strollers have been recalled, following dozens of reports involving problems where the strollers unexpectedly collapsed and the hinge mechanism caused lacerations, resulting in nearly 20 injury reports.ย The Qbit stroller recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on December 20, following at least 71 reports of strollers problems involving sudden folding inward and another five reports of the hinge mechanism pinching caregiver and childrenโs hands, resulting in four lacerations, 12 contusions, and two broken bones.The CPSC indicates that the stroller’s design leads to fall and pinch hazards. The pinch hazard, responsible for the laceration injuries, is due to a gap within the hinge between the stroller seat and frame. The strollers also may unexpectedly fold and collapse due to an unlocking hinge. To date, of the 71 reports of the strollers collapsing, 12 children and adults have experienced minor bumps or bruises and one caregiver’s fall resulted in a fractured wrist and elbow.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 an estimated 29,400 gb Qbit lightweight strollers designed for children up to 50 pounds with model numbers 10AW1G-AQU2U, 10AW1G-RAS2U, 10AW1G-WHT2U, 10AW1G-CHA4U or 10AW1G-CIR5U. The gb Qbit models were manufactured for use as standard strollers and for travel systems with infant carriers. The strollers are equipped with four sets of two wheels, a five-point harnessed restraint system, a full-sized reclining seat, a storage basket, a removable cup holder, and a travel storage bag.The strollers are primarily black with accent colors including aqua, raspberry, white, charcoal or citrus lemon, and have the โgbโ red box logo printed on the harness and on both sides of the stroller legs along with the brand name โQbitโ printed in white on the stroller legs. Customers may locate the model number and manufacturing date printed on a sticker, located on the rear leg of the stroller directly above the wheels.The strollers were manufactured in China under Aria Child Inc. of Dedham, Massachusetts from March 25, 2015 through March 9, 2016. They were sold at Babies R US and other retail stores nationwide and online at Albeebaby.com, Amazon.com, Dmartstores.com, Medbroad.com and various other online retailers from May 2015 to November 2016 for about $180.Customers are being asked to stop using the recalled strollers immediately and contact Aria Child toll-free at 888-591-5540 or visit them online at www.ariachild.com and navigate to the โQbit Lightweight Stroller Recall Informationโ tab for information on how to receive a free replacement stroller. 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: Baby Stroller Recall, LacerationsMore Lawsuit Stories Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria November 3, 2026 Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026 Medtronic Insulin Pump Lawsuit Filed Over Recalled MiniMed 600 Series Device November 3, 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 Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: yesterday)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge 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) Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: 2 days ago)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026) Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 5 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)
Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026
Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: yesterday)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge 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)
Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: 2 days ago)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)
Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 5 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)