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.
Kids II Rocking Sleeper Recall Issued Due To Risk of Infant Deaths April 29, 2019 Russell Maas Add Your CommentsDue to concerns about a suffocation risk, a recall has been issued for nearly 700,000 additional infant “rocking” sleepers sold under brand names like Ingenuity, Bright Starts, Automatic and Disney Baby, which feature a design that is similar to certain Fisher-Price sleepers recalled earlier this month following at least 32 infant deaths.Nearly 700,000 infant inclined sleepers linked to several deaths in recent years have been recalled, due to a design which can lead to children suffocating after becoming trapped against the fabric.The Kids II Rocking Sleeper recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on April 26, due to a design that may cause infants to become trapped against the fabric if they are able to roll over.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 COMPENSATIONSince 2012, at least five infant deaths have been linked to the products, which come in addition to those associated with Fisher-Price Rock ‘N Play infant sleepers recalled on April 17.This new recall impacts approximately 694,000 models “Rocking Sleepers” that were sold under a variety of popular product names, including Ingenuity, Bright Starts, Automatic, and Disney Baby.The sleepers are similar to bassinets, except they are designed to elevate the babyโs head and torso to help prevent acid-reflux or congestion while sleeping. The sleepers are designed for newborns and infants unable to roll over on their own. However, parents will not know the exact moment a child gains that ability.The products are equipped with restraints intended to secure the infant from rolling over or turn on their side. However, if the infant becomes unrestrained, they may turn on their side, or roll completely over and not have the proper neck strength to lift their head, creating a suffocation risk.The sleepers were manufactured in China under Kids II, Inc. of Atlanta, Georgia. They were sold at major retailers nationwide, including Walmart, Target, Toys โRโ Us and also online from March 2012 through April 26, 2019 for between $40 and $80.Parents and guardians are being instructed not to put their infants in the sleepers and to stop using them immediately to prevent further injuries and deaths. Customers should contact Kids II at 1-866-869-7954 or visit their website online and click on โImportant Recall Informationโ.Prior to the Fisher-Price recall, the CPSC issued a Fisher-Price Rockโn Play warning on April 5, instructing consumers to stop placing their infants in the sleepers before they begin to show signs they can roll over independently.The American Academy of Pediatrics (AAP) issued a statement on April 9, calling for the commission to issue an immediate recall for the Rockโn Play Sleepers. The AAP determined the inclined sleepers were unsafe and that the CPSC warning did not go far enough to ensure the safety of infants.Following the AAPโs statement, Fisher-Price announced the recall of 4.7 million Rockโn Play Sleepers under the CPSCโs Fast Track recall process.Since the recall of Fisher-Price Rockโn Play sleepers, a number of individual wrongful death and class action lawsuits have been filed against Fisher-Price and Mattel, Inc. 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: Childrens Furniture, Childrens Furniture Recall, Infant Deaths, Infant Sleeper Recall, SuffocationMore Lawsuit Stories Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks October 1, 2026 Amazon Coowalk Heated Insoles Lawsuit Alleges Lithium-Ion Battery Explosion Caused Severe Burns October 1, 2026 Chlorpyrifos Ban Takes Effect Across EU as Studies Link Pesticide Exposure to Parkinsonโs Disease October 1, 2026 0 Comments FacebookThis 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 Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: today)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: yesterday)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) Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (Posted: 2 days ago)A Texas woman’s Boston Scientific SCS implant lawsuit claims she spent several years with a broken device in her back, but did not remove it because the company’s sales representatives said it just needed reprogramming.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (09/10/2026)
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Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: yesterday)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)
Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (Posted: 2 days ago)A Texas woman’s Boston Scientific SCS implant lawsuit claims she spent several years with a broken device in her back, but did not remove it because the company’s sales representatives said it just needed reprogramming.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (09/10/2026)