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.
ISMP Issues Analysis, Recommendations On Avoiding COVID-19 Vaccine Administration Errors April 27, 2021 Irvin Jackson Add Your CommentsA medication safety group says while errors administering the various COVID-19 vaccines are rare, the medication mistakes being made by doctors and other healthcare professionals vary greatly, but indicate some safety precautions could eliminate many of them.The Institute for Safe Medication Practices (ISMP) released a report on April 22, analyzing safety errors linked to the Pfizer-BioNTech, Moderna and Johnson & Johnson COVID-19 vaccines. It is their second review of the vaccine distribution. The first was in January, when vaccines began, and the second comes four months into the process, which has seen Americans receive 231 million doses, with about 96 million Americans fully vaccinated.According to the ISMP review, the largest number of general errors made with all types of vaccine include patients receiving a lower dose than authorized, and the vaccines being given to patients younger than the recommended ages.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 COMPENSATIONMany of the cases where patients received a lower dose than authorized were due to patients pulling away from the needle before the health care professional injecting them were finished. However, the report notes that at one mass vaccination clinic, about 4,300 patients received a 0.2 mL dose of the Pfizer vaccine, instead of the 0.3 mL dose they were supposed to receive. This occurred because the syringes from the national stockpile left about a third of the vaccine stuck in the bottom of the plastic syringe.The age-related problems occur generally when the vaccine providers fail to ask age-related questions.There are also a number of incidents which are specific to the two-dose vaccines by Pfizer and Moderna. In some cases, patients received the wrong vaccine for the second dose, and in other cases, they were given the doses during the wrong time intervals. Patients receiving the Pfizer vaccine have to wait at least 17 days between the two doses, and those receiving the Moderna vaccine have to wait at least 24 days. In some cases vaccines are given too soon, too late, or they received a third dose by accident.In many cases, these mistakes occur during the interview of patients before they receive their vaccines, ISMP found.The ISMP issued the following recommendations to help avoid the most common COVID-19 vaccine administration errors:Educate and orient all vaccination staff, including volunteers, on their role in vaccination check-ins, patient screening, preparation, administration and common errors that occur.Verify the competency of all vaccinatorsVerify competency of staff who screen and check-in patients.Schedule patients for a second dose, if needed, before they leave the vaccination site after receiving the first dose.Establish a scheduling system that does not allow patients younger than 16 to obtain an appointment.Ask patients age-related screening questions, including date of birth, and comply strictly with vaccine age restrictions.Check state and local databases for documentation of COVID-19 vaccinations for those requesting a first or second dose.Require all patients who arrive for a second dose to present their vaccine card and have them carry the card throughout the process.The ISMP also recommends pharmacies verify the number of vaccines needed each day and dispense prefilled, labeled syringes, separate the preparation of each brand of vaccine, and withdraw doses from one vaccine vial at a time before accessing the next vial, and label vaccine syringes immediately after preparation.The report also recommends that, during administration, each vaccine station be stocked with a sharps container for syringe and needle disposal, each syringe be checked for the proper dose, air bubbles, and a tight fit between the needle hub and syringe, and check patientsโ vaccine cards to verify correct time interval and manufacturer. In addition, those administering the vaccines should immediately engage the needle safety device and dispose of the syringe in a sharps container, report any syringe or needle malfunctions to the pharmacy, and be sure to complete the patientโs vaccine card.The ISPM also urges those administering the vaccine to have an independent double check of the Pfizer vaccine dilution process and stock vaccination sites with epinephrine autoinjectors to visually differentiate them from vaccine syringes.โMillions of doses of the COVID-19 vaccines will be administered over the next few months,โ the ISMP report states. โAs we work toward expanding vaccinations to all, we must also learn from the vaccine errors that have already happened and implement strategies to minimize the risk of making these same vaccine errors.โ Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Coronavirus, Medication Error, Prescription Mistake, VaccineMore Lawsuit Stories Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026 Indoor Fire Pit Lawsuit Indicates Flame Jet Set User’s Body on Fire August 20, 2026 Missouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit August 20, 2026 0 Comments X/TwitterThis 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 Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: today)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: yesterday)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) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026
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