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.
Bacterial Infection Outbreak at Nursing Homes and Hospitals Linked To Contaminated Syringes November 17, 2016 Russell Maas Add Your CommentsNursing home residents and hospital patients in at least five states have become infected with a specific strain of bacterium linked to a saline solution recall announced by federal health officials last month, resulting in several hospitalizations and potentially contributing to the death of at least six individuals.ย The U.S. Centers for Disease Control and Prevention (CDC) issued an update this week on a multistate outbreak of Burkholderia cepacia bloodstream infections, which have infected at least 151 individuals at 58 nursing homes and medical centers nationwide.The outbreak is linked to a Nurse Assist prefilled saline flush syringe recall announced last month by the FDA.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 COMPENSATIONNew Jersey has been the hardest hit by the outbreak. According to local news sources and the CDC, at least 13 new cases across New Jerseyโs Atlantic County and Ocean County have been reported since the recall, bringing the state’s total of infected patients to 52.Investigations by health officials have revealed that many long-term care or nursing home facilities used the contaminated saline solution syringes prior to the recall. Currently, Maryland, New York, Delaware, Pennsylvania and New Jersey all have confirmed cases of B. Cepacia believed to be linked to the syringes.The recall involved syringes that are prepackaged saline flushes used in a healthcare setting to administer intravenous treatments, clearing central or arterial lines of any medicine or perishable liquids that could pose a sterilization hazard.Manufacturing company Nurse Assist Inc., in conjunction with the FDA, recalled any and all unexpired lots of the Nurse Assist I.V. Flush Syringe products that were distributed to customers and distributors between February 16, 2016 and September 30, 2016. The recalled products were sold in 3ml sizes with Product Code 1203, 5ml sizes with Product Code 1205, 10ml sizes with Product Code 1210, and 10ml sizes with Product Code 1210-BP. Product Numbers 1203, 1205, and 1210 were packaged 30 syringes to an inner carton and six inner cartons in a case totaling 180 syringes. Product Number 1210-BP was packaged with 400 syringes to a case.Burkholderia cepacia is a group of complex bacteria that can be found in soil and water and is often resistant to many common antibiotics, posing an increased risk to those with weakened immune systems such as children and the elderly.Although the bacterial infection poses no significant threat to healthy individuals, those with respiratory infections, specifically cystic fibrosis and chronic lung disease may be more susceptible to the bacteria and require immediate medical treatment.Common symptoms of the bloodstream infection include fevers, chills, clammy skin, shortness of breath, and abnormal heart rates among other side effects. Healthcare facilities known to have received and administered the recalled saline solutions to patients are being asked to monitor patients for side effects. 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 nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Burkholderia Cepacia, Hospital Infection, Infection, Medical Device Recall, Nursing Home, SyringeMore Lawsuit Stories Lawsuit Alleges Roblox Sexual Predator Convinced 8-Year-Old Girl To Send Him Explicit Videos May 14, 2026 Ozempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk May 14, 2026 Gourmia Pressure Cooker Lawsuit Alleges Lid Interlock Failure Caused Life-Altering Burn Injuries May 14, 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 Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: yesterday)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026) Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: 2 days ago)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026) Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 3 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)
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