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.
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
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.
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.
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.
Fisher-Price Rock ‘n Play Sleeper Recall Reannounced After Additional Infant DeathsAn additional 70 infant deaths have been linked to recalled Fisher-Price Rock ‘n Play Sleepers, which continue to be used by families despite the serious suffocation risks the design poses January 10, 2023 Russell Maas Add Your CommentsFederal safety officials have re-announced a Fischer-Price recall that impacted nearly 5 million “Rock โn Play” infant sleepers, after receiving dozens of additional reports of infants becoming trapped and suffocating to death against the fabric years after the products were removed from the market.The U.S. Consumer Product Safety Commission (CPSC) posted new information about the Fischer-Price infant sleeper recall on January 9, 2023, warning that many consumers are placing their childrenโs life at serious risk by continuing to use the recalled inclining sleepers.Infant suffocation risks have been linked to a number of inclined sleeping products sold in recent years, including rockers, gliders, soothers, and swings. However, concerns over the design of Fisher-Priceโs Rock โn Play sleepers were first raised in early 2019, after the products were linked to at least 30 infant fatalities.According to the latest update, the CPSC has now become aware of an additional 70 infant deaths involving inclining sleeper products. The agency stated that Fisher-Price has been investigating the reported incidents and in some of the cases has been unable to confirm the circumstances or whether the product was a Rock โn Play Sleeper.Fischer-Price Rock nโ Play Sleeper RecallIn early April 2019, the CPSC first raised concerns over the inclining design of Fischer-Price Rock โn Play infant sleepers, warning consumers to stop placing infants in the sleepers before they begin to show signs that they can roll over independently. Officials warned that infants may have the ability to roll over on their stomach and become trapped against the inclined bed, creating a suffocation risk.Shortly after the initial CPSC warning, the American Academy of Pediatrics (AAP) issued a statement, calling for the commission to issue an immediate recall for the Rockโn Play Sleepers. The AAP determined the inclined sleepers were unsafe, and that the CPSC warning did not go far enough to ensure the safety of infants.Just 12 days after the warning, the agency issued a Fisher-Price Rock โn Play Sleeper recall, impacting approximately 4.7 million units. The recalled included all models of Rock โn Play sleepers that were distributed for sale throughout the United States to major retailers for between $40 and $149 since 2009.BABY FORMULA NEC LAWSUITSWas your premature child fed Similac or Enfamil?Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONBABY FORMULA NEC LAWSUITSWas your premature child fed Similac or Enfamil?Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONFischer- Price Rock โn Play LawsuitsFollowing a nearly two year investigation after the recall, a House Oversight Committee reportย was released in June 2021, alleging Fisher-Price failed to adequately vet the Rockโn Play inclined infant sleeper for safety before putting it on the market in 2009, and indicating the manufacturer intentionally ignored pre-market warnings and concealed reports of infant deaths to avoid issuing costly recalls.The report also revealed Fisher-Price and its parent company, Mattel Inc., were aware of dangers posed by the 30 degree inclining sleepers well before the products were available to consumers. According to the findings, the companyโs internal safety committee raised alarms about the dangers posed by an inclined sleeper as early as 2008.According to the report, Fisher-Price had documented at least 14 infant deaths in the sleepers by February 2018, which is more than a year prior to publicly recognizing any potential risks to consumers, and allegedly never reported the deaths to the CPSC.Since the recalls, Fisher-Price has been hit with a number ofย inclined sleeper individual wrongful death lawsuitsย and at least 10 class action lawsuits alleging the manufacturer knew or should have known about the risk of problems, yet delayed announcing a recall or warning, and knowingly allowed parents to continue purchasing life-threatening sleeper devices. 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: Children Furniture Recall, Fisher-Price, Infant Deaths, Infant Sleeper Find Out If You Qualify for Infant Formula NEC CompensationMore Baby Formula Lawsuit Stories Court Rejects Appeal in Similac Special Care Lawsuit Over NEC Warnings July 30, 2026 Similac Injury Lawsuit Alleges Newborn Developed NEC After Being Fed Cow’s Milk-Based Formula July 20, 2026 Premature Infant Formula Lawsuit Alleges Enfamil Caused Necrotizing Enterocolitis (NEC) July 1, 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 Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: today)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
Similac Injury Lawsuit Alleges Newborn Developed NEC After Being Fed Cow’s Milk-Based Formula July 20, 2026
Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: today)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)
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Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)