Order Requires Valsartan Recall Lawsuits To Provide Product Identification for Specific Generic Drug Makers Named
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.
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.
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
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
AngioDynamics Port Catheter 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.
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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
AFFF Lawsuit Exposure to firefighting foam chemicals may result in an increased risk of cancer for firefighters, military and airport personnel.
Paraquat Parkinson’s Disease Lawsuits Exposure to the toxic herbicide Paraquat has been linked to a risk of Parkinson's disease.
Graco Inclined Sleeper Recall Issued Due to Risk of Infant Death December 17, 2020 Russell Maas Add Your Comments Federal 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 baby’s 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 child’s chin down to his or her neck, creating an airway blockage. Do You Know about… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The recalled sleepers include the inclined accessory sold with the Graco Pack ‘n Play Day2Dream Playard with Bedside Sleeper with model numbers 2034085, 2048753 and 2053215,  Graco Pack ‘n Play Nuzzle Nest Playard with model numbers 1947177 and 1896392, Graco Pack ‘n Play Everest Playard with model numbers 1946902 and 1946903, and Graco Pack ‘n Play Rock ‘n 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 Children’s 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 Risks Inclined infant sleeper safety concerns were first made public in April 2019, when the CPSC 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. 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-Price’s recall of 4.7 million Rock’n Play Sleepers and a 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 of 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), 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 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. Tags: Children Furniture Recall, Graco, Inclined Sleeper, Infant Death More Lawsuit Stories Ozempic Delayed Gastric Emptying Led to Stomach Paralysis: Lawsuit March 27, 2025 Order Requires Valsartan Recall Lawsuits To Provide Product Identification for Specific Generic Drug Makers Named March 27, 2025 Benzene From Gas Ovens Increase Childhood Cancer Risks: Study March 27, 2025 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermNameThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Ozempic Delayed Gastric Emptying Led to Stomach Paralysis: Lawsuit (Posted: today) A Mississippi woman’s Ozempic lawsuit indicates that she suffered stomach paralysis due to the drug’s delayed gastric emptying side effects, which left her with permanent injuries. 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MORE ABOUT: BARD POWERPORT LAWSUITSmiths Medical Port Catheter Recall Issued Over Manufacturing Error (03/20/2025)E. Coli Infection Was Caused by AngioDynamics SmartPort Port Catheter, Lawsuit Alleges (03/03/2025)Schedule To Prepare Bard PowerPort Lawsuits for Bellwether Trials To Be Proposed by Parties (02/27/2025)
Order Requires Valsartan Recall Lawsuits To Provide Product Identification for Specific Generic Drug Makers Named March 27, 2025
Ozempic Delayed Gastric Emptying Led to Stomach Paralysis: Lawsuit (Posted: today) A Mississippi woman’s Ozempic lawsuit indicates that she suffered stomach paralysis due to the drug’s delayed gastric emptying side effects, which left her with permanent injuries. MORE ABOUT: OZEMPIC LAWSUITCourt Urged To Reject Motion To Dismiss Lawsuits Over Ozempic, Mounjaro Gastrointestinal Risks (03/21/2025)GLP-1 Manufacturers Argue Gastroparesis Lawsuits Should Require Contemporaneous Diagnostic Testing (03/17/2025)Study Suggests There May Not Be a Link Between Ozempic, Mounjaro and Post-Surgery Aspiration Pneumonia (03/12/2025)
Court Clears BioZorb Lawsuit Design Defect Claims Over Recalled Breast Tissue Marker (Posted: yesterday) A U.S. MORE ABOUT: BIOZORB LAWSUITGroup of 7 BioZorb Injury Lawyers Appointed to Leadership Positions in Lawsuits Over Recalled Breast Tissue Marker (03/19/2025)Breast Cancer Survivors File Lawsuit Over Recalled BioZorb Tissue Marker (03/12/2025)BioZorb Attorneys Propose Leadership Structure for Lawsuits Over Recalled Tissue Marker (03/05/2025)
Bard PowerPort Bellwether Trial Selections To Be Made in Late April 2025 (Posted: yesterday) Parties have until April 28 to turn in a list of six Bard PowerPort lawsuits that should be prepared for bellwether trials. MORE ABOUT: BARD POWERPORT LAWSUITSmiths Medical Port Catheter Recall Issued Over Manufacturing Error (03/20/2025)E. Coli Infection Was Caused by AngioDynamics SmartPort Port Catheter, Lawsuit Alleges (03/03/2025)Schedule To Prepare Bard PowerPort Lawsuits for Bellwether Trials To Be Proposed by Parties (02/27/2025)