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 Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
Fisher-Price Rock ‘n Glide Soothers Recalled Following Infant Deaths June 7, 2021 Russell Maas Add Your CommentsFollowing the deaths of at least four babies, more than 200,000 Fisher-Price infant sleepers are being recalled, due to a dangerous design that may cause an infant to suffocate or become entrapped against the fabric if they are able to rollover onto their stomach.The U.S. Consumer Product Safety Commission (CPSC) announced a Fisher-Price 4-in-1 Rock ‘n Glide Soothers recall on June 3, instructing consumers to stop placing infants and children in the sleepers immediately, to prevent asphyxiation and suffocation risks.The recalled devices are part of a class of products referred to as inclining infant sleepers, which are designed to elevate the baby’s head and torso. Inclining the infant during sleep has been shown to help prevent acid-reflux or congestion. However, the design can be deadly for babies old enough to rollover on their own, or if the incline of the bassinet forces the child’s chin down to his or her neck, creating an airway blockage.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 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 COMPENSATIONAccording to the CPSC notice, the agency has become aware of at least four infant suffocations occurring in the recalled Fischer-Price inclined sleepers, including deaths of a 4-month old from Missouri, a 2-month old from Nevada, a 2-month old from Michigan and an 11-week old from Colorado between April 2019 and February 2020.The recall specifically includes Fischer-Price 4-in-1 Rock ‘n Glide Soothers with model numbers CHP56, CHP55 and CBT81, and 2-in-1 Soothe ‘n Play Gliders with model numbers GDD28, GDD39, GDD41, GGW85, GNX43, GVG43, HBD26 and HBD27. The sleepers contain a powered glider seat and an infant rocker which can move in a head-to-toe or side-to-side motion.CPSC officials indicate approximately 120,000 4-in-1 Rock ‘n Glide Soothers and 55,000 2-in-1 Soothe ‘n Play Gliders were sold at juvenile product stores and mass merchandisers nationwide and online, including Walmart and Target stores and Amazon.com. The Rock ‘n Glide Soothers were sold from January 2014 through December 2020, for about $108, while the 2-in-1 Soothe ‘n Play Gliders were sold from November 2018 through May 2021, for about $125.An additional 25,000 4-in-1 Rock’n Glide Soothers and an estimated 27,000 2-in-1 Soothe’n Play Gliders were distributed for sale to various retailers in Canada.Fischer-Price is instructing customers to stop using the recalled products immediately and to contact the manufacturer at 855-853-6224 or visit them online at www.service.mattel.com for information on how to receive a refund.Inclined Sleeper Safety ProblemsThe CPSC first raised concerns over inclined sleepers in April 2019, when it issued a Fisher-Price Rock’n Play warning, instructing consumers to stop placing their infants in the sleepers by three months old, or before they begin to show signs that they can roll over independently.By June 2019, CPSC officials had become aware of at least 32 infant deaths, with 18 additional deaths identified after the initial warnings, bringing the total number of deaths to approximately 50. The agency announced that between January 2019 and December 2020, a total of 254 incidents related to inclined sleep products were reported.Shortly after the warning, a series of recall were announced, including 4.7 million Rock’n Play Sleepers and 694,000 Kids II inclined rocking sleepers. Fisher-Price subsequently issued another recall impacting 71,000 of its Price Ultra-Lite Day & Night Play Yards.Just last week, the CPSC voted 3 to 1 to approve a new infant sleep product rule, which will require all products marketed for infant sleep to meet new mandatory safety standards/ These standards will require new and existing infant sleep products to not exceed a 10 degree incline to avoid entrapment hazards which increase the risk of suffocation.The new standard will also require inclined sleepers, travel and compact bassinets, and in-bed sleepers which do not already meet the requirements of an existing CPSC sleep standard to be tested and removed from the market if not compliant. 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 nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Entrapment, Fisher-Price, Inclined Sleeper, Infant Deaths, Infant Furniture, SuffocationMore Lawsuit Stories Amazon Nitrous Oxide Death Lawsuit Set for Trial in December 2027 August 28, 2026 TikTok Settlement Over Child Privacy Violations Results in $400M Payment August 28, 2026 Harbor Freight Transmission Jack Failure Lawsuit Filed Over Crushing Hand, Arm Injuries August 28, 2026 0 Comments PhoneThis 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 Amazon Nitrous Oxide Death Lawsuit Set for Trial in December 2027 (Posted: yesterday)A federal judge has scheduled a nitrous oxide wrongful death lawsuit trial against Amazon.com for December 2027.MORE ABOUT: NITROUS OXIDE LAWSUITWhippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters (08/14/2026)Flavored Nitrous Oxide Lawsuit Alleges Amazon Canisters Caused Woman’s Death (05/27/2026)Social Media Influencers Promote Nitrous Oxide Use Without Warning About Inhalation Risks (05/18/2026) Olympus Colonoscopy Lawsuit Over C. 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Amazon Nitrous Oxide Death Lawsuit Set for Trial in December 2027 (Posted: yesterday)A federal judge has scheduled a nitrous oxide wrongful death lawsuit trial against Amazon.com for December 2027.MORE ABOUT: NITROUS OXIDE LAWSUITWhippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters (08/14/2026)Flavored Nitrous Oxide Lawsuit Alleges Amazon Canisters Caused Woman’s Death (05/27/2026)Social Media Influencers Promote Nitrous Oxide Use Without Warning About Inhalation Risks (05/18/2026)
Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (Posted: 2 days ago)An initial status conference is slated for September 29 to discuss an Olympus colonoscopy lawsuit claiming the company’s medical cameras spread infectious materials from one patient to another.MORE ABOUT: SCOPE INFECTION LAWSUITEndoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026)Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)
Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (Posted: 3 days ago)The JPML will hear oral arguments in late September over whether to consolidate all federal Abbott Laboratories and Nevro spinal cord stimulator lawsuits for coordinated pretrial proceedings.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (08/18/2026)Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)