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.
Kelloggs Special K Cereal Recall Issued Over Glass Fragments February 22, 2013 Russell Maas Add Your CommentsAbout 36,000 boxes of Kellogg’s Special K Red Berries Cereal have been recalled, due to the risk that there may be small glass fragments in the cereal, which could pose a serious risk of mouth and digestive system injuries for consumers.ย The Kellogg’s Special K recall was announced on February 15, after Kellogg Company learned that glass fragments may have contaminated the cereal during the manufacturing process. While no injuries have been reported to date, consumers are being asked to not eat the cereal.The recall consists of Kellogg Company Special K Red Berries cereal sold in 3 different sizes across the United States with the following UPC Code and “Best Used By” dates: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 COMPENSATION11.2 ounce packages, UPC code 3800059923 with a Better if Used Before Date of DEC 02 2013 followed by KNC 105 with a time stamp of 00:13-2:3022.4 ounce packages, UPC code 3800078356 with a Better if Used Before Date of NOV 30 2013 followed by KNA 105 with a time stamp of 07:00-08:51 and a Better if Used Before Date of NOV 30 2013 followed by KNB 105 with a time stamp of 15:00-17:0537 ounce packages, UPC code 3800020940 with a Better if Used Before Date of NOV 30 2013 followed by KNB 107 with a time stamp of 17:31-20:05The Kellogg’s Special K Cereal products sold in sizes other than 11.2, 22.4 or 37 ounces are not being recalled and are not suspected to have glass fragments within.This recall comes just a few months after a Kellogg Mini-Wheats recall was issued in October 2012, after the discovery of fragments of flexible metal mesh that came from a faulty manufacturing part.Kellogg’s is advising consumers to check their cereal boxes to verify if it has been recalled and to contact Kellogg’s Consumer Affairs at 1-800-962-1413 or email them by visiting http://www.kelloggs.com/en_US/contact-us.html 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: Cereal Recall, Kelloggs, Special K 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 CompanyThis 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: yesterday)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: 2 days ago)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. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)Endoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026) Cartiva Injury Lawyers Appointed to Leadership Roles in Federal MDL (Posted: 3 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)
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: yesterday)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: 2 days ago)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. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)Endoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026)
Cartiva Injury Lawyers Appointed to Leadership Roles in Federal MDL (Posted: 3 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)