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.
Surgeons Leaving Tools Behind in Patients is Not Rare: Report October 22, 2013 Irvin Jackson Add Your CommentsA 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. ย 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…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 COMPENSATIONMost 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 towelsDevice components and fragments, like stapler components, guidewires, catheters and broken partsNeedles and other sharpsMalleable retractors and other instrumentsThe 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 JacksonSenior Legal Journalist & Contributing EditorIrvin 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 SpongeMore Lawsuit Stories Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway October 14, 2026 Lawsuit Alleges Apple AirTag Tracker Used to Monitor Womanโs Location October 14, 2026 Heart Valve Lawsuit Alleges Abbott Trifecta GT Failed Years Earlier Than Expected October 14, 2026 0 Comments NameThis 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 Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: today)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) GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (Posted: yesterday)A Florida manโs lawsuit claims he became legally blind after developing NAION while using the diabetes drug Ozempic.MORE ABOUT: OZEMPIC LAWSUITOzempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (09/08/2026) Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (Posted: 2 days ago)Boston Scientific SCS implant litigation is moving toward a process that will speed up future lawsuit filings as the number of claims continues to rise.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott 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)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)
Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (Posted: today)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)
GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (Posted: yesterday)A Florida manโs lawsuit claims he became legally blind after developing NAION while using the diabetes drug Ozempic.MORE ABOUT: OZEMPIC LAWSUITOzempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (09/08/2026)
Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (Posted: 2 days ago)Boston Scientific SCS implant litigation is moving toward a process that will speed up future lawsuit filings as the number of claims continues to rise.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott 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)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)