MDL Sought for LโOreal Class Action Lawsuits Over CeraVe, Other Benzoyl Peroxide Products Contaminated With Cancer-Causing Chemicals
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.
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
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.
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.
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.
Banana Boat Hair & Scalp Sunscreen Recall Issued Over Cancer RiskBenzene found in Banana Boat sunscreen may pose health risks for consumers, and comes after a series of sunscreen recalls issued in recent years due to the cancer-causing chemical in aerosol spray cans August 1, 2022 Russell Maas Add Your CommentsA recall has been issued for several batches of Banana Boat sunscreen, after the spray was found to contain dangerous levels of benzene, which is a chemical classified as a human carcinogen that has been discovered in a number of aerosol sunscreen products in recent years.The U.S. Food and Drug Administration (FDA) announced theย Banana Boat Hair & Scalp sunscreen recall on July 29, after routine sample testing confirmed the presence of potentially unsafe levels of the benzene in several brands of aerosol spray cans.Benzeneย is an industrial chemical that has been associated with the development of several fatal forms of cancer, leukemia and other conditions, such as AML, Chronic Myelogenous Leukemia (CML), Acute Lymphocytic Leukemia (ALL), Chronic Lymphocytic Leukemia (CLL), Hairy Cell Leukemia (HCL), Non-Hodgkinโs Lymphoma, Multiple Myeloma, Myelodysplastic Syndrome (MDL), Myelofibrosis and Myeloid Metaplasia, Aplastic Anemia and Thrombocytopenic Purpura.According to the U.S. Department of Health and Human Services (DHHS), side effects of benzene exposure may increase the risk of cancer, and the chemical has long declared it is linked to fatal forms of leukemia and other cancers. The FDA considers it a solvent that should not be used in drug products, if avoidable. However, if benzene is not avoidable, it should be restricted to 2 ppm, FDA regulations state.The Banana Boat recall comes after a number of similar aerosol sunscreen spray products have been found to contain high levels of benzene, including Neutrogena, Aveeno, Coppertone and others. As a result, a dozens of sunscreen cancer lawsuits have been filed by individuals diagnosed with lymphoma following regular use of the spray over large portions of their body.Stay Up-to-Date AboutSunscreen lawsuitsStay up-to-date about developments in benzene lawsuits over the presence of the harmful chemical in a spray sunscreens, deodorants and other products by subscribing to the AboutLawsuits Weekly Digest. "*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date AboutSunscreen lawsuitsStay up-to-date about developments in benzene lawsuits over the presence of the harmful chemical in a spray sunscreens, deodorants and other products by subscribing to the AboutLawsuits Weekly Digest."*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreThe manufacturers of the recalled Banana Boat sunscreen, Edgewell Personal Care Company, told the FDA that benzene is not an intended ingredient in the products, but an internal review of samples identified the presence of trace amounts of the chemical, which was formed from the propellant that sprays the sunscreen out of the cans.The recall includes three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 that are marked with UPC code 0-79656-04041-8 and lot codes 20016AF, 20084BF or 21139AF. The recalled sunscreen products are packaged in 6 ounce aerosol cans and were distributed nationwide through various retail channels.Edgewell has notified its retailers of the potential benzene contamination and has instructed stores to stop selling the products and to remove them from stores shelves.Consumers are being instructed to stop using the recalled Banana boat sunscreen spray products immediately and to properly discard them. Customers who purchased the recalled sunscreen products will be offered a reimbursement.The FDA is encouraging customers to report any adverse reactions or quality problems with the recalled Banana Boat sunscreen to the agencyโs MedWatch Adverse Event Reporting program either online, by regular mail or by fax.Spray Sunscreen Benzene ProblemsConcerns about high levels of benzene in sunscreen spray first emerged in May 2021, when the on-line pharmacy Valisure issued a warning thatย benzene was detected in 78 sunscreen and after-sun care productsย tested from their inventory.Following the report, Johnson & Johnson issued anย Aveeno and Nuetrogene sunscreen recall and just a few months later aย Coppertone sunscreen recall was issued for similar benzene contamination problems.Another Banana Boat sunscreen recall was later issued in December 2021, after internal testing discovered the benzene contamination in Banana Boat Ultra Very High Protection Clear Sunscreen Spray SPF, Banana Boat Simply Protect Kids Very High Protection Sunscreen Lotion Spray SPF 50+ and Banana Boat Dry Balance Very High Protection Clear Sunscreen Spray SPF 50+.At the forefront of the sunscreen litigation, at least eight class action lawsuits filed against Johnson & Johnson were centralized for coordinated management as part of a federal MDL, or multidistrict litigation, in the U.S. District Court for the Southern District of Florida.In October 2021, a Johnson & Johnson sunscreen settlement was reached to resolve the centralized class action lawsuits, which all raised similar allegations that consumers developed various forms of blood cancers following regular use of recalled Neutrogena or Aveeno products. 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: Banana Boat, Benzene, Cancer, Chemicals, Sunscreen, Sunscreen Recall Image Credit: Image via <a href="http://www.flickr.com/photos/booleansplit/">booleansplit</a> via <a href="http://creativecommons.org/licenses/by/2.0/" target="_blank" rel="noopener">Flickr CC by 2.0</a>More Sunscreen Recall Lawsuit Stories JPML Refuses To Consolidate Lawsuits Over Benzene in LโOreal CeraVe, Other Acne Products February 14, 2025 MDL Sought for LโOreal Class Action Lawsuits Over CeraVe, Other Benzoyl Peroxide Products Contaminated With Cancer-Causing Chemicals January 3, 2025 Manufacturer to Remove Benzene-Linked Chemical from Generic Mucinex Due to Cancer Concerns August 23, 2024 0 CommentsX/TwitterThis 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
JPML Refuses To Consolidate Lawsuits Over Benzene in LโOreal CeraVe, Other Acne Products February 14, 2025
MDL Sought for LโOreal Class Action Lawsuits Over CeraVe, Other Benzoyl Peroxide Products Contaminated With Cancer-Causing Chemicals January 3, 2025
Manufacturer to Remove Benzene-Linked Chemical from Generic Mucinex Due to Cancer Concerns August 23, 2024
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)