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.
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
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.
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.
Livestock Antibiotic Use to be Limited by FDA Due to Human Health Risks December 12, 2013 Martha Garcia Add Your CommentsFederal health officials hope to phase out the use of antibiotics to encourage the growth of livestock, citing growing resistance among humans to antibiotic drugs as a major reason for the need to limit use of the drugs on food-producing animals.On December 11, the FDA issued draft guidance for a voluntary plan to limit the use of certain antibiotic drugs for enhanced food production. The plan calls for antibiotics to be used for therapeutic uses only, instead of as growth enhancers.The agency is concerned about the widespread use of antibiotic drugs among livestock, which may be jeopardizing human health by creating a resistance to these drugs.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 COMPENSATIONThe guidance requests pharmaceutical companies who manufacture antibiotic drugs for food producing animals to revise the FDA approved conditions on drug labels. The new program will also create changes to the Veterinary Feed Directives (VFD) process, the system which governs the distribution and use of drugs.The changes will phase in veterinary oversight, as opposed to over-the-counter availability, for the use of antibiotic drugs for therapeutic uses in food producing animals. Once the changes have been made, using antibiotics for growth will no longer be allowed.The FDA is asking companies to notify the agency within the next three months of their intention to participate. If so, the companies will then have three years to fully implement the changes outlined.The guidance outlines a plan that will be entirely voluntary, as officials believe a voluntary plan is the โfastest, most efficient way to make these changes.โAntibiotics are often added to animal feed or drinking water to help cattle, poultry and hogs gain weight faster or use less food to gain weight. The concern is antibiotics may contribute to the development of human resistance to the same drugs. Antibiotic resistance can be transferred to humans who eat food from the animals receiving the drugs.Growth-promoting antibiotic use in food providing animals has been under major scrutiny in recent years.In August, Merck announced the launch of a study focusing on the health risks of Zilmax, a popular cattle supplement used to increase cattle weight. The decision came after cattle which had been given Zilmax exhibited difficulty walking and movement. The company has indicated that the decision was made based on animal welfare, but critics point to Zilmax as the culprit of the animal lameness.Some have criticized the voluntary nature of the plan, indicating that there is no incentive, positive or negative, for companies to participate.Officials recommend antibiotics should only be used when medically necessary. Approximately 70 percent of medically important antibiotics sold in the United States are used on food producing animals.Last year, the FDA was ordered by a U.S. judge to begin eliminating the use of antibiotics on farms. Prompted by the growing concern of antibiotic-resistance infections in humans, the FDA was required to begin eliminating non-medical use of antibiotics like, penicillin and tetracycline antibiotics.Recently, the CDC issued a statement calling the use of antibiotics in animals to promote growth as unnecessary and calling for the drugs to be phased out. According to CDC estimates, more than 23,000 people a year are dying from drug-resistant infections. 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: Antibiotics, ZilmaxMore Lawsuit Stories Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits August 21, 2026 Sexual Predator Groomed Teen Boy on Roblox Using Robux, Lawsuit Alleges August 21, 2026 AngioDynamics Xcela Port Lawsuit Alleges Infection, Migration Caused by Defective Catheter August 21, 2026 0 Comments PhoneThis 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 Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits (Posted: 2 days ago)Abbott Laboratories has agreed to pay $670 million to resolve more than 2,000 Similac NEC injury lawsuits, as the first federal NEC trial against competitor Mead Johnson gets underway.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITMissouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit (08/20/2026)Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week (08/11/2026)Neocate Infant Formula Lawsuit Alleges Nutritional Defect Caused Rickets, Bone Fractures (08/05/2026) Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: 3 days ago)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026) FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: 4 days ago)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026)
AngioDynamics Xcela Port Lawsuit Alleges Infection, Migration Caused by Defective Catheter August 21, 2026
Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits (Posted: 2 days ago)Abbott Laboratories has agreed to pay $670 million to resolve more than 2,000 Similac NEC injury lawsuits, as the first federal NEC trial against competitor Mead Johnson gets underway.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITMissouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit (08/20/2026)Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week (08/11/2026)Neocate Infant Formula Lawsuit Alleges Nutritional Defect Caused Rickets, Bone Fractures (08/05/2026)
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