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 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
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.
FDA Warns of Morphine Overdoses Due To Medication Errors January 11, 2011 Staff Writers Add Your CommentsA morphine solution manufactured by Roxane Laboratories, Inc., which was only approved one year ago, has already been tied to a number of morphine overdoses and deaths, leading federal regulators to issue a warning to consumers and causing the drug maker to create a new label to avoid dosage confusion.ย The FDA issued a morphine overdose safety alert on Monday, warning that serious adverse events and deaths have been linked to overdoses of morphine sulfate oral solutions from Roxane Laboratories. Most of the cases appear to have been due to someone misreading the label of the 100 mg/5mL doses, confusing the milligrams (mg) for milliliters (mL).When milligrams are mistaken for milliliters, the dosage a patient receives could be 20 times stronger than what was intended, likely resulting in a drug overdose. In some overdose cases a 5 mg dose was administered as a 5 mL dose, which is equal to 100 mg. Roxane has agreed to change its labeling as a result of the confusion.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 new labels will have a warning that reads โONLY FOR USE IN PATIENTS WHO ARE OPIOID TOLERANTโ and the 100 mg per 5 mL dosage indication will be followed by (20 mg/mL). This is to distinguish it from the companyโs 20 mg/5 mL product. The more powerful dosage will also have white lettering on a red background to differentiate it from weaker doses.Roxaneโs morphine sulfate oral solution was approved by the FDA in January 2010 for the treatment of moderate to severe acute and chronic pain. It was part of the FDAโs unapproved drugs initiative. The initiative was designed to address a number of painkillers that were being released in strengths that had not been approved by the FDA. A number of generic morphine, oxycodone, hydromorphone and roxanol manufacturers were ordered to stop making extremely potent doses of painkillers until they got approval from the FDA.In recent years, prescription drug poisoning has surpassed automobile accidents as the leading cause of unintentional injury death among people between the ages of 35 and 54. According to research released last year from the West Virginia University School of Medicine, there was a 65% increase in prescription drug overdoses between 1999 and 2005, commonly involving overdoses of morphone, OxyContin and fentanyl. Tags: Fentanyl, Hydromorphone, Medication Error, Morphine, Morphine Overdose, Oxycodone, OxycontinMore Lawsuit Stories Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria November 3, 2026 Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026 Medtronic Insulin Pump Lawsuit Filed Over Recalled MiniMed 600 Series Device November 3, 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 Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: today)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge 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) Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: yesterday)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026) Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 4 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)
Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026
Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: today)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge 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)
Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: yesterday)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)
Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 4 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)