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.
Graco Inclined Sleeper Recall Issued Due to Risk of Infant Death December 17, 2020 Russell Maas Add Your CommentsFederal safety officials have announced a recall of more than 50,000 Graco inclined sleepers, due to design defects which may pose a risk of entrapment and suffocation for babies, after similar designs have been linked to dozens of infant fatalities.The U.S. Consumer Product Safety Commission (CPSC) announced the Graco inclined sleeper recall on December 16, after recognizing the products may increase the risk of infants becoming trapped or suffocating against the fabric if they roll over.Inclining infant sleepers and bassinets 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 potentially deadly for babies old enough to rollover on their own, or if the incline of the bassinet forces the childโs 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 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 recalled sleepers include the inclined accessory sold with the Graco Pack โn Play Day2Dream Playard with Bedside Sleeper with model numbers 2034085, 2048753 and 2053215, ย Graco Pack โn Play Nuzzle Nest Playard with model numbers 1947177 and 1896392, Graco Pack โn Play Everest Playard with model numbers 1946902 and 1946903, and Graco Pack โn Play Rock โn Grow Playard with model number 2105055.Officials indicate only the inclined sleeper accessory is being recalled, and customers may continue using the Playards and other associated accessories.The products were manufactured by in China and imported by Graco Childrenโs Products Inc., of Atlanta, Georgia. They were distributed for sale throughout the United States at Babies R Us, BuyBuyBaby and other stores nationwide and online at Amazon.com, Target.com and various other websites from May 2015 through September 2020 for between $270 and $350.Customers are being instructed to stop using the inclined sleeper accessories immediately and contact Graco at 800-345-4109 for a refund.Inclined Sleeper RisksInclined infant sleeper safety concerns were first made 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. The warning was issued after the CPSC publicly recognized at least 32 infant deaths related to the products.Since the warning, several manufacturers issued recalls of inclined sleeper products in April, including Fisher-Priceโs recall of 4.7 million Rockโn Play Sleepersย and aย recall of 694,000 Kids II inclined rocking sleepers. Fischer-Price subsequently released an additional inclined sleeper recall in June, impacting 71,000 inclined sleeping accessories sold with their Ultra-Lite Day & Night Play Yards.Fischer-Price has been riddled with a number ofย inclined sleeper wrongful death lawsuits and class action claims, 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.Following the series of recalls, the U.S. Public Interest Research Group (U.S. PIRG) released a survey in August 2019, finding at least 10% of child daycare facilities nationwide currently had one or more of the recalled infant beds in their possession, and were continuing to use the products on a daily basis.According to the U.S. Food and Drug Administration (FDA), aboutย 4,000 infants annually die unexpectedly during sleepย 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 American Academy of Pediatrics recommends infants sleep on their backs positioned on a firm, empty surface, not containing any soft objects toys, pillows or loose bedding. The recommendations call for new parents 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 nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Children Furniture Recall, Graco, Inclined Sleeper, Infant DeathMore Lawsuit Stories Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL August 24, 2026 Kratom Addiction Lawsuit Alleges Opioid-Like Products Caused Addiction, Cardiac Injury August 24, 2026 Clear Eyes Recall Issued Due to Risk Eye Drops May Be Contaminated August 24, 2026 0 Comments NameThis 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 Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (Posted: today)A federal judge has appointed a group of plaintiffs attorneys to leadership positions in the growing Boston Scientific spinal cord stimulator federal litigation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (08/18/2026)Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026) Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits (Posted: 3 days ago)Abbott Laboratories has agreed to pay $670 million to resolve more than 2,000 Similac NEC injury lawsuits, as the first federal NEC trial against competitor Mead Johnson gets underway.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITMissouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit (08/20/2026)Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week (08/11/2026)Neocate Infant Formula Lawsuit Alleges Nutritional Defect Caused Rickets, Bone Fractures (08/05/2026) Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: 4 days ago)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)
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