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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
CPSC Warns Parents to Stop Using Recalled Boppy Newborn Loungers Following Additional Infant DeathsFederal safety officials have become aware of 10 infant fatalities linked to the dangerous design of recalled Boppy Newborn Loungers. June 8, 2023 Katherine McDaniel Add Your CommentsFederal safety officials have issued renewed warnings for parents to stop using Boppy newborn loungers, which were recalled nearly two years ago, but continue to cause infants to suffocate and die.The U.S. Consumer Product Safety Commission (CPSC) issued a new Boppy infant lounger warning on June 6, indicating parents should stop using the products and be aware that some websites continue to illegally sell the recalled infant loungers on their platforms.The warning follows a recall of over 3.3 million Boppy newborn loungers first issued in September 2021, following at least eight reports of infants suffocating and dying after rolling over in the loungers between December 2015 and June 2020.The suffocation deaths occurred after the infants were reportedly placed in the loungers awake on their back, stomach, or side and were later found deceased on their side or stomach. Since then, the CPSC indicates it has received at least two more reports of infant deaths linked to the recalled infant loungers.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 COMPENSATIONThe Boppy newborn lounger recall impacted all models and colors of Boppy Original, Boppy Preferred, and Pottery Barn Kids Boppy newborn loungers sold online at Amazon.com, and in Pottery Barn Kids, Target, and Walmart stores. The loungers retailed between $30 and $44, and were distributed from January 2004 through September 2021.According to officials, the infant loungers pose a suffocation risk to infants, who can potentially roll or move off the pillows and place themselves in a position which inhibits their breathing. While the padded loungers were not intended to be used as infant sleep products, the agency determined that the products posed a great risk of suffocation to consumers and should not remain on the market.Additional Infant Deaths Linked To Recalled Boppy LoungersFollowing the recall announcement in September 2021, the CPSC received at least two additional reports of infant deaths linked to the Boppy newborn loungers, bringing the total of known deaths to ten. The first of the two reports was received in October 2021, after an infant rolled off the cushioned lounger and underneath an adult pillow nearby and died from positional asphyxiation. A month later, in November 2021, another infant, whose cause of death was undetermined, was found deceased after being placed on the lounger in an adult bed with soft bedding.The recalled loungers have been illegal to sell or donate since the recall was announced, however, the dangerous loungers continue to be sold through online platforms, including Facebook marketplace, despite numerous attempts from both the agency and Boppy for the recalled products to be removed from their sites.Despite continued infant suffocation deaths linked to infant loungers, and a study conducted in 2022 by the CPSC that highlighted the high risk of infants suffocating in the loungers, tighter regulations have yet to be implemented. Because infant loungers are not specifically marketed as infant sleep products and are considered safe for use when infants are awake, they avoid stricter CPSC oversight than the agency would implement for infant sleep products, and have therefore remained on the market.According to the U.S. Food and Drug Administration (FDA), approximately 4,000 infant fatalities occur annually due to accidental suffocation, and many of the reported suffocation deaths resulted from the infant rolling on their stomach or side after being placed in the lounger while awake.The CPSC emphasizes that babies should always be placed on their backs to sleep, and the safest place for a baby to sleep is on a flat, firm surface in a bassinet, crib, or play yard. Babies should not be exposed to blankets, pillows, crib bumpers, or any other items in their sleeping environment. Consumers are urged to participate in the recall and stop using the recalled Boppy newborn loungers immediately.Consumers may contact The Boppy Company by phone Monday through Friday from 9 a.m. to 5 p.m. ET at 800-416-1355, or online at www.boppy.com to receive a refund and instructions on how to properly dispose of their recalled products. Tags: Boppy, Infant Deaths, Infant Lounger Recall, Infant Sleeper, Suffocation Find Out If You Qualify for Infant Formula NEC CompensationMore Baby Formula Lawsuit Stories Enfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects March 12, 2026 Trial Over Similac Necrotizing Enterocolitis Injuries Underway in Chicago March 6, 2026 Lawsuit Alleges Premature Infant NEC Death Caused by Similac Formula January 21, 2026 0 Comments LinkedInThis 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 Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (Posted: yesterday)A new claim against Boston Scientific joins a growing number of spinal cord stimulator lawsuits alleging the systems have failed to relieve pain and instead worsened symptoms for many individuals.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMedtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026) 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates (Posted: 2 days ago)A federal judge has selected 10 hair relaxer lawsuits to serve as potential bellwether trials after altering the selection process to eliminate non-representative cases.MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (04/01/2026)Hair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026) High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: 3 days ago)A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026)
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