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 Sliced Cheese Recall Expanded Over Choking Hazards September 9, 2015 Russell Maas Add Your CommentsA recent recall for Kraft Singles cheese slices is being expanded to ten times its original size, following at least two new complaints of consumers choking on a clear plastic coating that may stick to the slices after being unwrapped.ย The Kraft sliced cheese recall expansion was announced by the manufacturer on September 3, including an additional 335,000 cases.The cheese slices may have a thin piece of plastic remain adhered to the cheese after the wrapper has been removed, posing a choking and suffocation hazard to consumers. To date, Kraft has received at least 12 consumer complaints of the plastic sticking to the cheese products, including five reports of consumers choking.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 initialย Kraft Singles recall was first announced by the FDA on August 3, including only about 36,000 cases. The company decided to expand the recall after it received the two new choking reports, in order to more accurately cover all potentially impacted products. The expansion brings the recall total to approximately 371,000 cases of American and White American Kraft Singles.The original recall included three and four-pound cases of Kraft American and White American Singles with manufacturing codes S54 and S55 with โBest When Used By Datesโ ranging from December 29, 2015 through January 4, 2016. The expanded recall now includes three and four-pound cases of Kraft Singles American and White American cheese product with “Best When Used by Dates” ranging from December 12, 2015 to March 2, 2016 and manufacturing codes S54 and S55. The โBest Byโ dates and manufacturing code are both stamped on the outer box and the individual packages.The products were manufactured by Kraft Heinz Company of Northfield, Illinois where they were distributed for sale in in the U.S., Puerto Rico, and 10 other countries and territories including Anguilla, the Bahamas, Belize, Bermuda, Grand Cayman, Netherlands Antilles, St. Kitts and Nevis, South Korea, St. Lucia, and the British Virgin Islands.Kraft is warning customers in possession of the recalled cheese products not to consume them, recommends returning the remaining portions to the store of purchase for an exchange or a full refund. Consumers within the U.S. and Puerto Rico may also contact Kraft Heinz Consumer Relations for a full refund by calling 1-800-432-3101 Monday through Friday 9 a.m. to 6 p.m. Eastern Time. 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: Cheese Recall, Choking, Kraft Image Credit: |More Lawsuit Stories Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss September 8, 2026 Torax LINX Lawsuit Scheduled for September 2028 Jury Trial September 8, 2026 Lawsuit Seeks Kratom Addiction Warnings, Corrective Advertising September 8, 2026 0 Comments FacebookThis 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 Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026) Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge 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)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026) Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: 6 days ago)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. 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Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: yesterday)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 5 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge 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)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: 6 days ago)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)Endoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026)