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.
Fisher-Price Inclined Sleeper Recall Issued for Ultra-Lite Day & Night Play Yards June 28, 2019 Russell Maas Add Your CommentsAmid continuing concerns about a growing number of infant deaths linked to inclined sleepers, a number of products have been pulled from the market due to the risk that infants may role over independently and become entrapped or suffocate.A Fisher-Price inclined sleeper recall was announced by the U.S. Consumer Product Safety Commission (CPSC) this week, for more than 70,000 accessory units used with Ultra-Lite Day & Night Play yards.Inclining infant sleepers are similar to bassinets, but are designed to elevate the babyโs head and torso. Inclining the infant during sleep has been shown to help prevent acid-reflux or congestion. However, the design has proven to be potentially deadly after babies are old enough to rollover on their own.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 inclined sleepers that were sold with the Fisher-Price Ultra-Lite Day & Night Play Yards, which were also equipped with changing station clutch accessories and a carry bag. The inclined sleepers marked with model numbers CBV60, CHP86, CHR06, CJK24, and DJD11 that were printed on a fabric label located inside of the inclined sleeper pad.The products were manufactured by Fisher-Price of East Aurora, New York. They were distributed for sale at juvenile product stores and mass merchandisers nationwide from October 2014 through June 2019 for between $90 and $110.Customers are being asked to stop using the inclined sleeper accessory immediately and to contact Fisher-Price at 800-432-5437 or visit their Recalls & Safety Alert page for additional information on how to receive a full refund.Inclined Sleeper Warnings Follow Infant DeathsThe recall follows a slew of infant inclined sleeper products that have been deemed unsafe for infants.Inclined sleeper safety concerns were disclosed to the public in April 2019, when the CPSC issued a Fisher-Price Rockโn 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.In response to the warning, the American Academy of Pediatrics (AAP) challenged the commissions warning indicating parents will not know the exact moment a child gains the ability to roll over, which may be too late and result in another infant death.By the end of April, CSPC officials recalled 4.7 million Rockโn Play Sleepers and Kids II recalled all 694,000 of its inclined rocking sleepers. While there were 32 infant deaths reported at that time, at least 18 additional deaths have surfaced over the past few months, bringing the total number of deaths to approximately 50.While some products have been recalled, and federal officials are considering a ban on inclined infant sleepers, the consumer watchdog group Consumer Reports urges parents and caregivers to stop using any and all rocking inclined sleepers.ASTM International, the voluntary industry standards organization, is investigating the products’ standards and potential hazards. It expects that review to be completed by October 2019, at which time it will decide whether to recommend if sleepers should be eliminated from the market.Since the recalls, Fischer-Price has been targeted by a number of inclined sleeper individual wrongful death lawsuits and also a class action lawsuit 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: Child Death, Childrens Furniture Recall, Class Action Lawsuit, Fisher-Price, Infant Deaths, Infant Furniture, Mattel, SuffocationMore Lawsuit Stories Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment October 2, 2026 Paraquat Settlement Offers Rejected by Hundreds of Parkinsonโs Disease Plaintiffs October 2, 2026 Walmart Expert Grill Brush Recall Impacts 4.4 Million Over Wire Bristle Ingestion Risk October 2, 2026 0 Comments URLThis 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 Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: yesterday)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026) Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: 2 days ago)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026) Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: 3 days ago)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)
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