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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
FDA Sends Letter to Canned Food Processors About Risk of Botulism July 24, 2008 AboutLawsuits Add Your CommentsThe FDA has recently posted a letter on their website which was sent several months ago to the canned food industry, warning about the risk of botulism which can develop from under-processed food products.The letter, which is dated December 21, 2007, was sent to highlight several recalls issued last year as a result of under-processed canned foods and to make members of the low acid canned food (LACF) industry aware of the serious public health risk posed by food poisoning which can result from manufacturing problems.During commercial canning of food, the cans are supposed to be heated long enough and at high enough temperatures to kill spores which could develop and grow. Manufacturing failures which result in the under-processing of canned food products can allow the survival and growth of the C. botulinum toxin, which thrives inside the sealed container. This poisonous toxin can lead to a serious and potentially fatal form of food poisoning, known as Botulism, if the food is consumed, inhaled or absorbed through the eyes or skin.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 COMPENSATIONBotulism causes muscle paralysis,and can result in blurred or double vision, difficulty swallowing and breathing, dizziness, nausea, slurred speech and weakness. When the toxin enters the body, it binds to nerve endings, blocking signals which leads to paralysis. Symptoms of botulism usually appear within 12 to 36 hours after exposure, but problems could develop in as little as two hours in some cases.Over the past thirty years, canned foods manufactured commercially have rarely, if ever been contaminated with botulinum bacteria. However, last year manufacturing problems led to several canned food recalls due to a risk of botulism. In July 2007, tens of millions of cans of chili, beef stew, corned beef hash and other meet products were recalled by Castleberry Food Company after cans produced at their Augusta, Georgia plant were not properly heated. In August 2007, Lakeside Foods, Inc. recalled cans of French cut green beans which were found to be contaminated with the C. botulinum bacteria.In the letter, the FDA also outlined several actions which they urged the canned food industry to implement to reduce the risk of canned food contamination and avoid potentially life threatening botulism food poisoning. Some of recommendations included:A competent process authority should review any change in venting, steam supply, plumbing, or spreader configuration of a retort before it comes under operation. Firms should also update all temperature distribution studies.The cause of spoilage must be investigated immediately and timely remedial measures should be taken.Firms should ensure thorough evaluation of process deviations and provision of records upon request during an FDA inspection.The FDA has also cautioned canned food processors to critically inspect their operations and ensure delivery of a safe product to the consumer. Field investigators have begun to focus on the preventive measures while conducting routine inspections. Tags: Botulism, Canned Food, Food Poisoning Image Credit: |More Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026
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Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)
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