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.
Tassimo Coffee Makers, Espresso Discs Recalled Over Burn Hazards February 10, 2012 Staff Writers Add Your CommentsReports of people being sprayed and burned by erupting hot liquid and coffee grounds has led to a massive recall involving more than 1.7 million Tassimo coffee makers and 4 million Gevalia, Maxwell House and Nabob espresso T Discs.ย The Tassimo Coffee Maker Recall and the Tassimo Espresso T Disc recall were announced by the U.S. Consumer Product Safety Commission (CPSC) on February 9, after more than 160 combined reports of the devices spraying hot liquid and 41 reports of second-degree burns.The burn victims include a 10-year-old Minnesota girl who was hospitalized after the hot liquid sprayed her in the face and neck, as well as a 2-year-old Canadian girl who also was burned in the face.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 CPSC warns that the espresso T discs can become clogged and spray hot liquid onto consumers and bystanders during or after brewing. The Tassimo single-cup coffee makers use the discs.The recall affects 835,000 Tassimo Single-Cup Brewers in the United States, and 900,000 in Canada.The brewers were sold under both the Bosch and Tassimo brand names and use plastic T Discs filled with coffee or tea to brew hot beverages. The machines have either “Bosch,” “Tassimo” or “Tassimo Professional” printed on the front of the brewer. The recalled Bosch brewers have model numbers beginning with TAS100, TAS200, TAS451, TAS46, or TAS651 and have date codes beginning with FD and within the range of 8806 through 9109. The recalled Tassimo Professional machines have a model number of TAS6512CUL and date codes beginning with FD and within the range of 8905 through 9109.Recalled Tassimo espresso T discs include 2.1 million packages sold in the United States and 1.9 million sold in Canada. They were sold in packages of eight or 16 espresso T discs under the Gevalia, Maxwell House and Nabob labels. Gevalia discs affected by the recall include the flavors Espresso, Espresso Decaffeinated, Cappuccino, Cappuccino Decaffeinated, Skinny Cappucino, Latte, Caramel Latte Macchiato, Mocha and Peppermint Mocha. The recalled Maxwell House discs include the flavors Espresso, Cafรฉ Collection Cappuccino, Cafรฉ Collection Crรจme Cappuccino, Cafรฉ Collection Skinny Cappuccino, Cafรฉ Collection Latte, Cafรฉ Collection Crรจme Latte and Cafรฉ Collection Caramel Latte Macchiato. Nabob discs affected by the recall include the flavors Espresso, Cappuccino, Decaf Cappuccino, Late and Skinny Latte. All of the affected discs have codes ending with 11213 through 12020. The code is printed on the foil lid and on the side of the package.The coffee makers and espresso discs were sold at department stores, mass merchandise and home improvement stores nationwide and on websites including www.tassimodirect.com. The coffee makers were sold from June 2008 through February 2012 for between $100 and $250. Professional models were also sold to hotels and food service providers, who are being contacted directly. The T discs were sold from August 2011 through February 2012 for between $8 and $11 per package.The CPSC recommends consumers stop using the coffee makers and discs immediately. Consumers with the coffee maker can contact the manufacturer for a free replacement T disc holder for the brewer. The T discs can be returned to the firm for a full refund. To get a refund or replacement, consumers can visit the website at www.tassimodirect.com/safetyrecall or call (866) 918-8763. Tags: Burn, Coffee Maker Recall, Gevalia, Maxwell House, Nabob, TassimoMore Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 5 Comments Kevin November 23, 2014 Just picked one of these up today, completely mint and unused, for twelve bucks — and now, this stuff comes up in a search. Is anybody still involved with the things? Mine is a TAS 451xUC if that helps. Do I need some sort of invention to keep from getting 2nd degree facial scars? Amy February 17, 2012 My grandson was burned by this,. He is 3 years old. Tassimo/Kraft has known they would blow up and apparently launched a media notification campaign. I am a registered user, they didn’t notify me and I didn’t see the adds. So I continued to use it. Now my little Cooper is afraid to go into the kitchen. They are responsible. They don’t replace anything because it is all recalled and they have idiots that answer the phone and give you no answers. I think it’s time for class action Elenita February 12, 2012 It’s ridiculous that I have to call back the toll free number to get the mailer for the defective t-disc. why can’t this be emailed automatically after I filled up all the information online. I never receive a letter, call or email regarding the recall. Barbi February 10, 2012 I can’t tell you how many times my disks would explode.The money I spent was crazy. I finally took it back to Zellers & they would’nt exchange it for me. Now I’m stuck with these new disks. JOANN February 10, 2012 i have the tassimo coffee maker tas 451xuc is that the one for recall LinkedInThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: yesterday)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 2 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet 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) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 3 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
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