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.
Bumble Bee Tuna Recall Expanded Due to Risk of Loose Seals on Cans March 11, 2013 Russell Maas Add Your CommentsFaulty seals on cans of Bumble Bee tuna and albacore may affect more than 51,000 cases of the canned foods, leading to recalls due to potential health risks consumers may face if they eat the fish meat after it has spoiled or become contaminated with bacteria.ย The Bumble Bee tuna recall was initially announced by the FDA on March 6, involving 22,500 cases containing between 24 and 48 cans in each case. The following day on March 7, Bumble Bee Foods LLC announced an expansion of the canned food recall, increasing the number of affected products after recognizing that a faulty manufacturing process may not have allowed seals to tighten to company standards.The recall now includes of Bumble Bee 5 ounce cans of Brunswick Brand chunk light tuna in water, Bumble Bee Brand chunk light tuna in water, Bumble Bee Brand chunk light tuna in vegetable oil and Bumble Bee Brand chunk white albacore. The recalled cans were distributed to various retailers nationwide from January 17 to ย March 6, with “best by” dates ranging from January 14, 2016 through January 18, 2016.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 COMPENSATIONTo date, no reports of illnesses or injuries have been reported, but if the fish has spoiled or the cans have been infiltrated by bacteria, the recall cans could pose serious adverse health consequences to consumers. The loose seals pose a heightened risk that bacteria and pathogens may enter the tuna. The cans of tuna also are presumed to be good for eating until 2016 which allows an abundance of time for the tuna to spoil and become contaminated.The FDA recommends that consumers stop eating the recalled cans of tuna immediately and check the “best by” dates on the can. If the cans are part of the recall they should be disposed of followed by contacting Bumble Bee Consumer Affairs at (800) 800-8572 to receive a full refund. 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: Bumble Bee Tuna, Tuna 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 2 Comments Cherlyn April 28, 2015 I purchased the 48 case of 5oz tuna. We made two batches of the tuna fish 4 cans each and my entire family became sick we could not figure it out until we all determined we had the tuna fis. Personally, Smith’s should have watched the recalls we bought these less than 2 weeks ago. Patricia March 23, 2013 I bought Bumble-bee solid white tuna and it is brown, atery and disgusting! I will never buy this product again nor will my friends. What is soy doing in this product? It states solid white albacore! 631-727-0568 I am reporting this product to consumer affairs! 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 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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