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.
Kraft Singles Cheese Slice Recall Issued Over Choking Hazard August 3, 2015 Irvin Jackson Add Your CommentsApproximately 36,000 cases of Kraft Singles, individually wrapped cheese slices, have been recalled after the manufacturer received reports of problems caused by the thin plastic film remaining on the cheese even after it had been unwrapped, including at least three report of consumers suffering a choking injury.ย The Kraft Singles cheese recall was announced by the FDA on July 31, after at least 10 consumer complaints were received where a thin strip of the individual packaging film remained adhered to the cheese slice. Included in the 10 reports, three individuals reportedly choked on the thin clear plastic.The recall includes three and four pound sizes of Kraft Singles American and White American pasteurized prepared cheese products, with best used by date of December 29, 2015 through January 4, 2016.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 cheese products contain the manufacturing code S54 or S55, representing either of the two production lines the cheese was processed through. The โBest When Used Byโ dates and manufacturing codes are located on a stamp on the 3 and 4 pound boxes and also in the enclosed individual one pound packages.For a full list of recalled cheese products, production codes, and expiration dates, please visit the recall notice linked above. Kraft announced that no other products are impacted by the potential layer of plastic film remaining on products.The FDA estimates that roughly 36,000 cases are impacted by the recall. The cheese was manufactured and process by Kraft Heinz Company of Northfield, Illinois where they were shipped to retailers in the U.S., Puerto Rico, and Grand Cayman. According to Kraft, the products from these production lines were not shipped to Canada.In Kraftโs press release, the company deeply apologized to its consumers and has asked them to stop consuming the recalled portion immediately and return it to the store of purchase for a full refund. Consumers in the U.S. and Puerto Rico may also contact Kraft Heinz Consumer Relations for a full refund at 1-800-432-3101. 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: Cheese Recall, Kraft Image Credit: |More Lawsuit Stories Nitrous Oxide Injury Lawsuit Filed Over B12 Deficiency, Long-Term Side Effects October 9, 2026 Port Catheter Lawsuit Filed After Infection Led to Sepsis, Death October 9, 2026 Ultra-Processed Food Consumption Linked to Heart Disease, Cancer, Diabetes and Death October 9, 2026 0 Comments EmailThis 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. 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