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.
Hospira Morphine Recall Issued Due to Overdose Risk April 19, 2012 Staff Writers Add Your CommentsOne lot of morphine has been recalled by Hospira, Inc. after reports suggest that some vials may be overfilled, which could lead to a life-threatening morphine overdose.ย The Hospira Morphine Sulfate injection recall was announced by the FDA and Hospira, Inc. on April 17, after at least one customer reported that two syringes were filled beyond the fill line.While the company indicates that it believes the incident was isolated, the entire lot of morphine has been recalled.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 COMPENSATIONA morphine overdose can cause respiratory depression, low blood pressure and death. However, there have been no injuries or illnesses linked to the morphine recall.The recall affects lot 10830LL of Hospira Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject, NDC 0409-1258-30. The morphine is sold in prefilled glass cartridges for use with the Carpuject Syringe system. Ten of the Carpujects are sold in each box.The recalled lot was sold in January to distributors and hospitals in Arizona, Colorado, Hawaii, Illinois, Indiana, Michigan, Minnesota, Ohio, Texas and Virginia. It has an April 1, 2013 expiration date.The recall comes a little over a year after Marc Hermelin, former CEO of KV Pharmaceutical Co. was sentenced to a month in jail and nearly $2 million in fines and forfeited earnings for failing to prevent his company from selling oversized Ethex morphine pills that exposed consumers to a risk of serious and potentially life-threatening injuries.The Ethex morphine recall was first issued in June 2008, after it was discovered that manufacturing problems allowed oversized pills to potentially be distributed to customers. Subsequent recalls were issued for additional lots of morphine and at least 30 other generic drugs manufactured by Ethex which may have contained up to twice the necessary amount of the active pharmaceutical ingredient.Any customers who have the syringes of morphine affected by this latest recall should quarantine them from their inventory and call Stericycle at (888) 912-7088 to arrange for the products’ return. Tags: Drug Recall, Morphine, Morphine Overdose, Overdose Image Credit: |More Lawsuit Stories DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data June 26, 2026 Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial June 26, 2026 Study Finds Dose Response Link Between Alcohol and Pancreatic Cancer June 26, 2026 0 Comments CompanyThis 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 DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data (Posted: 2 days ago)A proposed class action lawsuit alleges DraftKings secretly shared website visitors’ personal information with third-party data brokers to build consumer profiles without their consent. 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DraftKings Faces Class Action Lawsuit Over Sale of Consumer Data (Posted: 2 days ago)A proposed class action lawsuit alleges DraftKings secretly shared website visitors’ personal information with third-party data brokers to build consumer profiles without their consent.
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Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: 4 days ago)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)