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 Recalls Millions Of Rock ‘n Play Sleepers Following Dozens of Infant Deaths April 15, 2019 Russell Maas Add Your CommentsAs a result of design problems that have resulted in at least 32 infant deaths, nearly 5 million Fisher-Price Rock‘n Play Sleepers are being recalled, due to a risk that babies may suffocate after becoming trapped against the fabric if they roll over.The U.S. Consumer Product Safety Commission (CPSC) announced the Fisher-Price Rock’n Play Sleepers recall on April 12, days after the agency issued a warning that urged consumers to stop placing infants in the sleepers before they begin go show signs that they can roll over independently, and to completely stop use of the sleepers by the time an infant is three months old.The infant deaths appear to have occurred when infants rolled from their back to their stomach while in the sleepers, which are marketed under the “Rock’n Play” brand. The impacted sleepers are inclining, which are similar to bassinets, however they are designed to elevate the baby’s head and torso to help prevent acid-reflux or congestion while sleeping.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 COMPENSATIONThe Rock’n Play models include restraints to prevent an infant from being able to sit up or roll over. However, when a child is not fastened properly in the restraints, the infant may turn on their side, or roll completely over and not have the proper neck strength to lift their head, creating a suffocation risk.Shortly after the initial CPSC warning was released last week, the American Academy of Pediatrics (AAP) issued a statement on April 9, calling for the commission to issue an immediate recall for the Rock’n Play Sleepers. The AAP determined the inclined sleepers are unsafe and that the CPSC warning did not go far enough to ensure the safety of infants.“When parents purchase a product for their baby or child, many assume that if it’s being sold in a store, it must be safe to use,” AAP President Dr. Kyle Yasuda said in the statement. “Tragically, that is not the case. There is convincing evidence that the Rock ‘n Play inclined sleeper puts infants’ lives at risk, and CPSC must step up and take immediate action to remove it from stores and prevent further tragedies.”Following the AAP’s statement, Fisher-Price voluntarily announced the recall under the CPSC’s Fast Track recall process.The recall affects approximately 4.7 million Rock’n Play Sleepers manufactured in China under Fisher-Price, of East Aurora, New York. They were distributed for sale throughout the United States to major retailers for between $40 and $149 since 2009. The recall involves all Rock’n Play models.The CPSC instructs consumers to stop using the sleepers immediately and to contact Fisher-Price at 866-812-6518 or visit them online to view the Recalls & Safety Alerts for information on how to receive a refund or voucher.According to the FDA, about 4,000 infants annually die unexpectedly during sleep from accidental suffocation, sudden infant death syndrome, or unknown causes. Many of the reported fatalities are a result of suffocation from rolling on their sides or stomach.To reduce suffocation and accidental deaths, the AAP recommends infants sleep on their backs positioned on a firm, empty surface, not containing any soft objects toys, pillows or loose bedding. The recommendation for new parents is to always follow the ABCs of safe sleep: Alone on the Back in a bare Crib. 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: Child Death, Childrens Furniture, Childrens Furniture Recall, Fisher-Price, Infant DeathsMore Lawsuit Stories Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial September 9, 2026 Lawsuit Alleges Apple AirTag Tracked Vehicle Location for Months September 9, 2026 Chlorpyrifos Autism Link May Involve Immune, Inflammatory Gene Changes: Study September 9, 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 Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: today)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026) Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: today)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)