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.
Rare Powdered Baby Formula Associated Illness Reported in Two Infants December 2, 2008 AboutLawsuits Add Your CommentsAccording to the New Mexico Department of Health, two infants have developed a rare bloodstream and central nervous system infection known as Enterobacter sakazakii, which is associated with the use of powdered baby formula. One of the infants has died from the infection and the other remains hospitalized.E. sakazakii is a harmful bacterium that can cause an invasive infection, especially in newborn infants, premature babies or those with weak immune systems. If it infects the bloodstream, it can cause meningitis and lead to a potentially life-threatening inflammation of the intestines.There have only been about 120 cases of the rare infection recorded worldwide, and it is associated with a death rate between 40% and 80%.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 COMPENSATIONAccording to a December 1, 2008, statement by the New Mexico Department of Health, one baby girl from Lea County, New Mexico has been hospitalized with E. sakazakii and a baby boy from Otero County, New Mexico has died from the infection. Although the infants had different strains of the bacteria, the discovery of the two cases so close together has raised concerns.The U.S. Centers for Disease Control and Prevention (CDC) has previously associated the rare illness with the use of infant formula, and both infants were fed powdered formula along with other foods.The New Mexico Department of Health has warned parents to be cautious about using powdered baby formula while the investigation into the cause of the infections is in progress. They have recommended that breastfeeding is the best option, if possible, and a doctor should be consulted before trying a new formula or changing an existing one.ย The New Mexico Department of Health is reminding parents that baby formula should be prepared for consumption in small amounts, and that cleanliness and proper hygiene during preparation should be maintained. Any unused formula should be discarded within two hours of preparation, and leftover formula after a feeding should be thrown away within one hour. Prepared formula stored in a refrigerator should be used within 24 hours.ย Symptoms of E. sakazakii infection could include unstable body temperature, jaundice, irritability, poor feeding response and grunting respiration. Infants surviving the infection may experience infection of the central nervous system and neurological impairment.This latest baby formula scare follows news last week that trace amounts of the industrial chemical melamine were discovered in samples of some formula manufactured in the United States. High levels of melamine which contaminated baby formula in China this year, has been associated with six deaths and over 294,000 illnesses according to the latest figures released.The FDA has indicates that the trace levels of melamine found in U.S. baby formula remains safe for infants, and they have stressed that parents should not stop using powdered formula manufactured in the United States.There is no indication that the cases of E. sakazakii infection in New Mexico is in any way connected with melamine contaminated formula. Tags: Baby Formula, E. Sakazakii, Enterobacter Sakazakii, Infant Formula, Melamine, New Mexico Image Credit: |More Lawsuit Stories Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 September 11, 2026 DraftKings Lawsuit Indicates ‘Event Contracts’ Are Nothing More Than Sports Bets September 11, 2026 Social Media Wrongful Death Lawsuit Links Major Platforms to Child Suicides September 11, 2026 2 Comments JackieSparkle December 14, 2008 It’s both. E. skazakii has been found in between 4% and 14% of samples of powdered formula milk tested. If the formula is prepared correctly, ie with boiling water, cooled immediately under a running tap and used asap, there is little risk. It needs to be remembered that formula is not sterile and it is very important to prepare it safely. http://www.healthpromotionagency.org.uk/Resources/nutrition/pdfs/bottlefeed2006.pdf sandra V. December 2, 2008 I’m confused! Is the bacteria in the formula or is it the way the parents handled the formula. 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 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 3 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 4 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 5 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 3 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 4 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 5 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)