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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.
Capri Sun Wild Cherry Recall Issued After Cleaning Solution Discovered in Drink PouchesThe manufacturer has not identified the cleaning solution that led to the Capri Sun Wild Cherry Recall, and no details have been released about the nature of illnesses experienced and long-term health risks August 16, 2022 Martha Garcia Add Your CommentsFollowing a number of consumer complaints, a Capri Sun recall has been issued for “Wild Cherry” flavor, after the manufacturer acknowledged that the popular juice drink pouches may contain a cleaning solution.The Capri Sun Wild Cherry recall was announced by Kraft Heinz on August 12, but the manufacturer has not provided information about the source of the contamination or potential health risks the drinks may pose, especially among young children.The company indicates that the the Capri Sun drinks were contaminated with a cleaning solution used on food processing equipment, which got into the product on the production line in one factory. However, the problems were not discovered until several consumers complained about a “foul” tasting Capri Sun, including several reports involving severe vomiting and diarrhea after drinking the “juice”.Some recalled products may still be on store shelves, and parents are outraged that the manufacturer has not been transparent about exactly what chemicals may be in the drinks, and what illnesses or long-term health risks may be caused.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 COMPENSATIONThe recall affects 6.6-ounce pouches of Capri Sun Wild Cherry Flavored Juice Drink Blend with UPC code 0 8768400100 4. Manufacturer codes on the individual pouches are 25JUN2023 followed by a โWโ and the numbers 01, 02, 03, 04, 09, or 10; then by an โLโ and a number between 01 and 12; and finally, by four numbers between 0733 and 0900. For example, 25JUN2023 W01 L01 0733.The drink is sold by the carton. The product will have โBest When Used Byโ date of June 25, 2023, on the pooches and on the carton. The recall includes 5,760 cases, or more than 23,000 individual drink pouches, of cherry flavored Capri Sun juice drink blends.Those who have the affected Capri Sun drink pouches should throw them out or return any recalled products to the store where it was purchased, Kraft Heinz recommends. Consumers can contact Kraft Heinz customer service about the recall at 800-280-8252 for more information or for a refund. 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: Capri Sun Recall, Chemicals, Children, Children Food, Kraft HeinzMore Lawsuit Stories Lawsuit Alleges Andexxa Administered To Reverse Xarelto Effects Caused Near-Fatal Thrombotic Event May 28, 2026 Faberware Pressure Cooker Explosion Lawsuit Claims Defective Walmart Device Caused Severe Burn Injuries May 28, 2026 Impella CP Set With SmartAssist Warning Issued by FDA After Patient Death May 28, 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)
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