Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms
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.
Philips Avent Digital Video Baby Monitor Recall Issued Over Lithium Ion Battery Fire RisksSafety experts have raised concerns over the use of lithium-ion batteries in recent years, following hundreds of reports of overheating, fires, and deaths due to their use in various products. August 4, 2023 Martha Garcia Add Your CommentsNearly 13,000 Philips Avent video baby monitors are being recalled following reports of overheating and a risk of fires that may develop.The Consumer Product Safety Commission (CPSC) announced the Philips Avent Digital Baby Monitor recall on August 3, after Philips received at least 23 reports of video baby monitors overheating in Europe. Seven of those reports lead to minor injuries, including burns. So far, no incidents or injuries have been reported in the United States.The Philips Avent Video Baby Monitor is used to remotely watch over infants via a 3.5-inch color screen and a camera unit. It contains a rechargeable lithium-ion battery in the parent unit, which is the video monitor portion. The camera unit is placed in the infant or childโs room. If the battery overheats it can pose a serious safety risk for young children.BABY FORMULA NEC LAWSUITSWas your premature child fed Similac or Enfamil?Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONBABY FORMULA NEC LAWSUITSWas your premature child fed Similac or Enfamil?Premature infants fed Similac or Enfamil cow’s milk formula face an increased risk of necrotizing enterocolitis (NEC) or wrongful death.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe recall affects monitor models SCD630 and SCD843. The model numbers and production date codes are located at the bottom of the parent unit (the video monitor portion). The monitors and camera are white with Philip Avent printed on the front. The affected models were manufactured between March 2016 and December 2019.According to the CPSC, an estimated 12,850 recalled units were sold online at ToysRUs.com, Amazon.com, Walmart.com, Jet.com, and https://ww.usa.philips.com/ from March 2016 through January 2020 for between $120 and $200.The CPSC indicates consumers who own recalled Philips Avent Baby Monitors should stop using them immediately and contact the company about the recall or for an Avent Baby Monitor replacement. Consumers can contact Philips at 833-276-5311 or online at www.philips.com/video-babymonitor-recall.Lithium-Ion Battery RisksThe Philips Avent Baby Monitor is not the first product plagued by issues with faulty lithium-ion batteries, which have been repeatedly linked to fires which have led to injuries, property damage and death.In 2022, the CPSC issued a warning about the risks lithium-ion batteries in e-scooters and other micro-mobility devices pose to consumers after the agency received more than 200 reports of fires, overheating and other incidents across the U.S. The various incidents resulted in nearly 20 fatal injuries.The warning was sent to more than 2,000 manufacturers and importers of e-scooters and other e-bicycle devices due to poorly designed and manufactured lithium-ion batteries.Earlier this year, the non-profit group Electrical Safety Foundation International launched a safety campaign focused on raising awareness about the risks posed by lithium-ion batteries as thousands of reports of fires, injuries, and other damage continue to be linked to batteries used in e-scooters, hoverboards, e-bicycles, and other electronic mobility devices. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Baby Monitor, Baby Monitor Recall, Burn, Fire, Infant, Lithium Ion Batteries, Philips, Property Damage Find Out If You Qualify for Infant Formula NEC CompensationMore Baby Formula Lawsuit Stories Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 May 14, 2026 Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms May 8, 2026 Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil April 24, 2026 0 Comments PhoneThis 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 Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: yesterday)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) GalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (Posted: 2 days ago)Growing reports of GalaFLEX breast mesh complications have raised concerns about women who required explant surgery, revision procedures or implant removal after the synthetic mesh was used during breast augmentation, breast lift, implant revision or reconstruction surgery.MORE ABOUT: BREAST MESH LAWSUITGalaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025) Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 6 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)
Lawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms May 8, 2026
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: yesterday)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
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