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 Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
U.S. Divers Youth Snorkeling Mask Recall Issued Due to Cracking Lens Risk March 8, 2013 Russell Maas Add Your CommentsAbout 175,000 youth snorkeling masks are being recalled following reports of the eye pieces breaking under water, posing a potential laceration hazard. A U.S. Divers Youth Snorkeling Mask recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on March 7, after at least 17 reports were received of the lens cracking while submerged, including 7 reports indicating the consumer suffered cuts and scratches to the face. The CPSC determined that the masks represent a laceration hazard.The recall consists of about 44,000 Martinique LX Jr. Youth Snorkeling Mask Sets and about 130,000 Santa Cruz Jr. Youth Snorkeling Masks. Both models were marketed and sold under the U.S. Divers and Aqua Lung Sports Brand.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 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 COMPENSATIONThe Martinique LX Jr. masks were sold at Costco Wholesale stores nationwide from November 2010 through July 2011 for about $30. The mask sets contain fins, a snorkel, a tempered glass face mask with adjustable straps and buckles, and a silicone face skirt. The masks are blue with silver trim and have a U.S. Divers logo above the nose piece and on the tempered glass. “Wave” is printed on the outer edges of the buckles.The recalled Santa Cruz Jr. masks were sold at Academy, Dick’s, The Sports Authority and other retailers nationwide, including online at Amazon.com and other online retailers, from March 2011 through July 2012 for about $10 individually and $30 for a set. The masks have a single-pane of tempered glass and were sold individually or as a set with a snorkel and fins. This model also contains the U.S. Divers logo on the bridge of the mask and inside on the tempered glass. Only the Santa Cruz Jr. Youth Masks manufactured before October 2011 are included in the recall.Both recalled models were manufactured in Thailand by Aqua Lung Inc., of Vista, California and imported by Aqua Lung Inc. dba U.S. Divers, of Vista, California.The CPSC advises consumers to stop using the recalled masks immediately and contact U.S. Divers at (888) 606-6162 for a free replacement mask or visit them online at www.usdivers.com and navigate to the “Recall Notice” for more information. 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 nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Snorkeling Mask Recall Image Credit: |More Lawsuit Stories Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries September 4, 2026 Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks September 4, 2026 Roblox Grooming Lawsuit Alleges Defective Platform Exposed Child to Sexual Predator September 4, 2026 0 Comments URLThis 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 Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: today)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026) Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: yesterday)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. 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Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries September 4, 2026
Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks September 4, 2026
Roblox Grooming Lawsuit Alleges Defective Platform Exposed Child to Sexual Predator September 4, 2026
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: today)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
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Cartiva Injury Lawyers Appointed to Leadership Roles in Federal MDL (Posted: 2 days ago)A federal judge has appointed more than a dozen plaintiffs’ attorneys to serve in leadership positions in the developing Cartiva lawsuit litigation.MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Implant Lawyers To Meet With MDL Judge for Initial Conference in Aug. 2026 (06/30/2026)Failed Cartiva Implant Required Multiple Toe Surgeries, Lawsuit Alleges (06/11/2026)Cartiva Surgery Lawsuit Claims SCI Implant Failure Required Big Toe Fusion (05/26/2026)