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.
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.
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.
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.
AngioDynamics Port Catheter 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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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.
Surgeons Leaving Tools Behind in Patients is Not Rare: Report October 22, 2013 Irvin Jackson Add Your Comments A new report suggests that surgeons and other health care professionals leave medical devices inside of patients after surgery more often than is generall believed, particularly sponges and broken tool parts.  The Joint Commission published a Sentinel Event Alert (PDF) on October 17, calling for health care professionals to take action to prevent the unintended retention of foreign objects (URFOs), also known as retained surgical items (RSIs). These events occur when a surgeon accidentally leaves a medical tool inside a patient’s body once surgery is complete. According to The Joint Commission, there could be as many as 2,000 such incidents each year in the United States alone. Do You Know about… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Most medical professionals consider URFOs as “never events,” meaning there is no excuse for them ever happening. The Joint Commission, a medical watchdog group, found more than 770 reports of retained foreign objects in surgical patients from 2005 to 2012. They resulted in at least 16 patient deaths. However, the group believes that a vast number of cases are never reported and estimates that most likely there are 1,500 to 2,000 URFO cases in the U.S. each year. Out of the 770 plus incidents the group analyzed, the Joint Commission found that the objects most commonly left behind in patients include: Sponges and towels Device components and fragments, like stapler components, guidewires, catheters and broken parts Needles and other sharps Malleable retractors and other instruments The analysis showed that one of the most common factors in surgeons leaving tools behind in patients appears to be body mass index, suggesting that it is easier to lose medical instruments in larger patients. Other risk factors include urgent procedures, unexpected changes during an operation, multiple procedures involving multiple teams, and staff changes during operations. Patients undergoing an emergency operation were nine times more at risk of URFO than other patients, and patients undergoing a procedure that changed unexpectedly were at four times the risk. Many experts, including The Joint Commission, say that the use of a simple checklist that accounts for every tool before and at the end of surgery, before closing procedures, can help prevent most URFO incidents. The group also recommends inspection of instruments before and after use to make certain fragments were not left in the patient’s body. Surgical team communication, briefings and debriefings would also help, the group found. In cases where URFOs are suspected, like when the surgical count is incorrect, the entire surgical field should be radiographed before the patient is removed from the OR, the group suggests. According to a 2003 report published in the New England Journal of Medicine, there were about 1,500 cases a year in which a sponge or surgical tool was left behind after surgery. Approximately 88% of the cases involved a final count that was incorrect. In many cases, forgotten surgical sponges left after surgery are not discovered for a number or years, when patients begin suffering from unexplained symptoms. The difficulty in detecting the surgical mistake has led most states to allow exemptions to the statute of limitations for medical malpractice suits in cases where a foreign object is left behind during surgery. The Joint Commission estimates that each incident can cost an average of $166,000 including legal defense, indemnity payments and surgical costs that are not reimbursed by Medicare. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin 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. Tags: Medical Device, Medical Malpractice, Surgical Error, Surgical Sponge More Lawsuit Stories Lawyers Call for Hair Relaxer Cancer Lawsuit To Be Set for Trial January 28, 2026 Syngenta Settles Paraquat Parkinson’s Lawsuit as Trial Was Set To Begin in Philadelphia January 28, 2026 Otis Elevator Lawsuit Alleges Malfunction Caused Elevator To Descend Uncontrolled January 28, 2026 0 Comments CommentsThis 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 Lawyers Call for Hair Relaxer Cancer Lawsuit To Be Set for Trial (Posted: yesterday) Ahead of a case management conference this week, hair relaxer cancer lawsuit lawyers have asked a federal judge to set a date for the first bellwether trial. MORE ABOUT: HAIR RELAXER LAWSUITPresentations on How Hair Relaxers Cause Cancer Will Be Heard by MDL Judge This Week (01/05/2026)Hair Relaxer Manufacturers Push for Evidence Many Plaintiffs Did Not Likely Keep (12/10/2025)Hair Relaxer Lawsuit MDL Status Hearings Scheduled Throughout 2026 (11/13/2025) Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: 2 days ago) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025) Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 3 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020)
Syngenta Settles Paraquat Parkinson’s Lawsuit as Trial Was Set To Begin in Philadelphia January 28, 2026
Lawyers Call for Hair Relaxer Cancer Lawsuit To Be Set for Trial (Posted: yesterday) Ahead of a case management conference this week, hair relaxer cancer lawsuit lawyers have asked a federal judge to set a date for the first bellwether trial. MORE ABOUT: HAIR RELAXER LAWSUITPresentations on How Hair Relaxers Cause Cancer Will Be Heard by MDL Judge This Week (01/05/2026)Hair Relaxer Manufacturers Push for Evidence Many Plaintiffs Did Not Likely Keep (12/10/2025)Hair Relaxer Lawsuit MDL Status Hearings Scheduled Throughout 2026 (11/13/2025)
Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: 2 days ago) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025)
Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 3 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020)