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.
Chlorpyrifos Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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
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.
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.
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.
Hospira Injection Recall Issued Due to Particulate Matter April 29, 2013 Russell Maas Add Your CommentsOne lot of Hospira’s sodium chloride injection has been recalled following a consumer complaint of particulate matter, which could pose serious and potentially life-threatening heath risks. A Hospira .09%Sodium Chloride Injection recall was announced by the FDA on April 26, after four different contaminants were identified within the injection solutions following testing of four individual containers.The Hospira injection contamination that was identified within the fluid consisted of polyester fiber, nylon fiber, cotton fiber, and nitrocellulose fiber.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 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 COMPENSATIONThe injections were originally recalled in August 2012, and this notice was a re-announcement of the action. However, Hospira Inc. has not received any reports of adverse consequences reported in relation to the solutions.The recall consists of .09% Sodium Chloride Injection 100 ml in flexible containers with lot number 05-201-JT. The recalled fluids were manufactured by Hospira Inc. and have an expiration date of May 1, 2013. The product was distributed to the following states to wholesalers, distributors, hospitals, and pharmacies: Alaska, Alabama, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and WyomingUse of the contaminated fluids may cause several health consequences such as local inflammation, phlebitis, or weakened immune systems. The risk to the consumer is heightened if the bacteria travels throughout the body and causes inflammation in the lungs.Consumers have been advised to stop using and distributing the product immediately and contact Stericycle at 1-888-597-9582 where they will inform the consumer to quarantine any remaining inventory until they can arrangement to remove and replace the product. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Drug Recall, Hospira, Particulate Matter Image Credit: |More Lawsuit Stories Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges October 16, 2026 Olympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities October 16, 2026 Dupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment October 16, 2026 0 Comments InstagramThis 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 Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: today)A Georgia woman’s spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026) Dozens File Joint Nitrous Oxide Addiction Lawsuit Against Amazon, Third-Party Retailers (Posted: yesterday)A joint nitrous oxide addiction lawsuit accuses Amazon and numerous third-party retailers of knowingly selling nitrous oxide for illegal recreational use.MORE ABOUT: NITROUS OXIDE LAWSUITNitrous Oxide Injury Lawsuit Filed Over B12 Deficiency, Long-Term Side Effects (10/09/2026)Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks (09/04/2026)Nitrous Oxide Sales Restrictions Pass California Legislature Amid Growing Abuse Concerns (09/02/2026) Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: 2 days ago)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)
Olympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities October 16, 2026
Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: today)A Georgia woman’s spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)
Dozens File Joint Nitrous Oxide Addiction Lawsuit Against Amazon, Third-Party Retailers (Posted: yesterday)A joint nitrous oxide addiction lawsuit accuses Amazon and numerous third-party retailers of knowingly selling nitrous oxide for illegal recreational use.MORE ABOUT: NITROUS OXIDE LAWSUITNitrous Oxide Injury Lawsuit Filed Over B12 Deficiency, Long-Term Side Effects (10/09/2026)Amazon, Online Nitrous Oxide Sellers Face Class Action Lawsuit Over Health and Safety Risks (09/04/2026)Nitrous Oxide Sales Restrictions Pass California Legislature Amid Growing Abuse Concerns (09/02/2026)
Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: 2 days ago)A federal judge has scheduled a fourth Bard PowerPort bellwether trial to begin on December 1, while the third trial is slated to begin on October 13.MORE ABOUT: BARD POWERPORT LAWSUITJudge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)