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.
Egg Manufacturers Warned About Violating Salmonella Prevention Rules January 14, 2013 Martha Garcia Add Your CommentsWarning letters issued by the U.S Food and Drug Administration (FDA) to two major egg producers detail a number of violations of rules, which are designed to prevent salmonella food poisoning.ย The FDA issued letters Midwest Poultry Services and SKS Enterprises, Inc. last month, which were released by the agency last week.Each letter details numerous violations of salmonella prevention rules that were found during inspections of facilities between May and August 2012.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 COMPENSATIONMidwest Poultry Services, based in Mentone, Indiana, produces nearly 150 million dozen eggs a year. According to FDA inspectors, the company failed to adequately implement requirements which would protect the eggs from contamination. The producer was cited for failing to implement a Salmonella prevention plan, use adequate methods for rodent control in poultry houses.According to inspections done in July, more than 100 rodents were caught at the facility within a five day period. Midwest Poultry also failed to rodent monitoring procedures and documentation detailing the new procedures.Among other violations, the company also failed to properly comply with egg refrigeration guidelines. Eggs which were grown at the facility are required to receive refrigeration within 36 hours of laying; however, the FDAโs record indicated refrigeration was not occurring within the 36 hours.Another major egg producer, SKS Enterprises, Inc., also received an FDA violation letter detailing multiple infractions, risking contamination of the eggs at their Lodi,ย California facility. SKS houses nearly 2 million laying hens and serves on the American Egg Board to promote the โIncredible Edible Eggโ campaign for the egg industry.The FDA inspected five of SKSโs egg production facilities and found numerous violations of the Salmonella Prevention Plan. Among the violations, SKS failed to conduct environmental testing during specified times. The company also failed to conduct the environmental testing used to detect Salmonella and used improper sampling and testing methods.In addition, multiple SKS facilities were in violation of having nearly 30 wild birds in their poultry houses. These facilities also reportedly had large six inch gaps along the roofing of the poultry enclosures, allowing wild birds and other animals to enter the facility and contaminate the eggs. SKS informed the FDA they would repair the gaps with chicken wire, but failed to submit detailed reports explaining how and when the action would be taken.Other documentation issues include failing to adequately maintain records detailing rodent and other pest prevention methods, and failing to submit written responses to the FDA concerning the inspections and violations.The issues identified at both Midwest Poultry and SKS violate the Salmonella Enteritidis in Shell Eggs During Production Storage and Transportation Regulations, a two year-old prevention rule implemented to reduce the risk of contamination instead of addressing it after it has occurred.According to the warning letters, the egg producers have 15 days from receipt of the letters to respond to the FDAโs inquiry and submit documentation specifying the steps and corrective action taken to address the violations and prevention methods to ensure contamination does not occur again in the future.Failure for either producer to correct the violations will result in FDA regulatory action, which can include seizure, injunction or administrative enforcement procedures. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: California, Eggs, Indiana, Salmonella Image Credit: |More Lawsuit Stories Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit May 22, 2026 Roblox Investigation Into Child Exploitation Problems Sought by Advocacy Groups May 22, 2026 Amazon Hand Warmers Lawsuit Claims Defective Products Sparked Fire Leading to Womanโs Death May 22, 2026 0 Comments EmailThis 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 Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 2 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-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)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026) Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: 3 days ago)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimerโs Disease Risks Questioned in New Study (04/27/2026) Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: 4 days ago)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)
Amazon Hand Warmers Lawsuit Claims Defective Products Sparked Fire Leading to Womanโs Death May 22, 2026
Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 2 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-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)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)
Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: 3 days ago)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimerโs Disease Risks Questioned in New Study (04/27/2026)
Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: 4 days ago)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)