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.
Porter Adventist Hospital in Denver May Have Exposed Patients To HIV, Hepatitis, State Officials Warn April 6, 2018 Irvin Jackson Add Your CommentsColorado health officials are warning that numerous patients treated at a Denver hospital may have been exposed to HIV and hepatitis, due to a sterilization breach.ย The Colorado Department of Public Health and Environment (CDPHE) issued a warning on April 4, indicating that the agency is working with Porter Adventist Hospital to notify patients that they were potentially exposed to infectious materials if they had orthopedic or spine surgery there between July 21, 2016 and February 20, 2018. However, neither the hospital nor health officials have yet received any reports of patients actually being infected.According to the warning from Dr. Larry Wolk, executive director and chief medical officer of the CDPHE, Porter Hospital’s process for cleaning surgical instruments following orthopedic and spine surgeries was found to be inadequate, “which may have compromised the sterilization of the instruments.”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 warning indicates that patients treated during the time period may have been exposed to HIV, hepatitis B or hepatitis C. However, the CDPHE also notes that the risk of one of these infections is very low. The risk that the sterilization breach may have caused other surgical site infections is unknown.The state’s health department is currently conducting a disease control investigation. It was first notified of the breach on February 21 and conducted an on-site survey of the hospital’s infection control practices the following day.The advisory notes that the practices at the hospital currently meet infection control standards. The last inspection to confirm those practices was March 28.“Porter Adventist Hospital stopped using and reprocessing all surgical equipment in question Feb. 20,” the CDPHE statement indicates. “While there is always a risk of infection during surgery, it appears there is no increased risk to current patients having surgery at Porter Adventist Hospital because of the infection control breach.”The hospital began mailing letters to patients who may have been at increased risk of infection on April 4. The hospital has not said how many patients have been mailed the notification letters.Porter Adventist Hospital noted that it paused all surgeries again on Thursday as a precaution, after noticing a potential change in its water quality, relative to its surgical equipment, according to a statement by the hospital on April 5. The hospital has published a list of Frequently Asked Questions related to the sterilization breach and its latest pause in surgical procedures. 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. 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