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.
PDI Alcohol Wipe Recall: Bacterial Contamination Risk September 22, 2011 Staff Writers Add Your Comments Another company has decided to recall its line of non-sterile alcohol prep pads and wipes due to the risk of bacterial contamination. Professional Disposables International, Inc. (PDI) announced an alcohol wipe recall on September 20, after Bacillus cereus bacteria was detected on some of its non-sterile prep pads. The same organism was responsible for problems that led to a massive alcohol prep pad recall earlier this year for Triad wipes manufactured by H&P Industries. Both alcohol wipe manufacturers reportedly share a common supplier. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION H&P Industries was shut down earlier this year after an FDA investigation into sanitary problems at its Wisconsin manufacturing facility found a number of issues. Contaminated Triad wipes made by H&P Industries have been linked to at least 8 deaths, 11 cases of infection and more than 250 consumer complaints. There have been no reported illnesses linked to contaminated PDI alcohol wipes. Bacillus cereus is responsible for about two percent of all foodborne illness, according to the U.S. Centers for Disease Control and Prevention (CDC). Illness comes within 24 hours after exposure and can result in a diarrheal illness. Serious illness and permanent injury are very rare. The PDI wipe recall affects all lots for six product lines, including PDI Alcohol Prep Pads,, Proadvantage Alcohol Prep Pads, Medi-Pak Alcohol Prep Pads, Medi-Choice Alcohol Prep Pads, ShopRite Alcohol Prep Pads and Duane Reade Alcohol Prep Pads. The recalls affect only the non-sterile versions of those pads. The company claims that the recalled products were manufactured under current Good Manufacturing Practices and tested prior to shipping. PDI also states that the company has updated product specifications and is conducting pre-shipping tests on all of its pads and wipes. A full list of item numbers and a lot number search engine have been posted in the PDI recall notice. Consumers with questions can call (800)999-6423 (ext. 8240) or send an e-mail to productsuport@pdipdi.com. The company has also posted a Recall Response Form (pdf) for customers with products that need to be returned. Tags: Alcohol Prep Pad, Alcohol Wipe, Bacillus Cereus Infection, Infection, PDI Alcohol Wipe Recall, Triad Image Credit: | More Lawsuit Stories Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain April 3, 2026 Lawsuit Claims Covidien Hernia Mesh Perforated Man’s Bowel April 3, 2026 Judge Upholds $9M Crock-Pot Pressure Cooker Lawsuit Verdict April 3, 2026 0 Comments URLThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 2 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026) Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 3 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026) Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: 4 days ago) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 2 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 3 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)
Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: 4 days ago) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)