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.
Cryofreeze, Arctic Zone Gel Pack Recall Expanded Due to Ingestion Fears June 12, 2012 Staff Writers Add Your CommentsAbout 880,000 freezer packs sold under the Cryofreeze and Arctic Zone brand names have been recalled, due to a risk that they may leak the gel contained inside and cause severe illness if ingested.The ice gel pack recall was posted by the U.S. Consumer Product Safety Commission (CPSC) on June 7, representing an expansion of a prior recall issued earlier this year for about 300,000 of the packs sold with lunch boxes and food carriers.According to the U.S. CPSC, the freezer gel packs, which were manufactured in China and imported by California Innovations, Inc., may leak gel if they become damaged. The gel inside the freezer packs contain diethylene glycol and ethylene glycol, which could cause illness if ingested in large amounts.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 COMPENSATIONWhen ethylene glycol metabolizes, common side effects include altered mental status and highly toxic blood levels resulting in hyperventilation and acidemia.Although there have been no new reports of injuries or incidents, the previous recall was issued after the importer received at least two separate reports of dogs chewing on the packs and ingesting the gel from the pack. One of the dogs died after ingesting the gel, and the other recovered after receiving medical treatment.The recalled products include ice/hot packs produced under the Cryofreeze or Arctic Zone labels.ย Specifically, units recalled involve the following packs distributed between July 2007 and December 2008:Cryofreeze ice/hot packs in small and large styles.Both have opaque blue wrappers with the words “Cryofreeze,” “Ice Pack/Hot Pack,” “Non-toxic” and “Reusable” printed on the front:The small gel pack is 6 inches wide and 5.5 inches highThe large gel pack is 8.5 inches wide and 8 inches highCryofreeze Transparent Cell ice/hot packs in three styles.Each has a transparent wrapper with the words “Cryofreeze,” “Ice Pack/Hot Pack,” “Non-toxic” and “Reusable” printed on the front:One 3-cell pack has three connected rectangular-shaped pouches of blue gel and is 7.85 inches wide and 5.5 inches high.Another 3-cell pack has three connected square-shaped pouches of blue gel and is 7.6 inches wide and 3 inches high.The 2-cell pack has two connected square-shaped pouches of blue gel and is 5 inches wide and 3 inches high.Arctic Zone ice pack is 6.25 inches wide and 4 inches high and has an opaque blue wrapper. The Arctic Zone logo and a picture of an iceberg appear on the front of the wrapper. The words “ICE,” “Personal Ice Pack” and “Non-Toxic Leak Proof Gel” are also printed on the front of the wrapper.The U.S. CPSC recommends that consumers immediately stop using the recalled freezer gel packs and contact their local waste disposal authority for instructions on disposing of them. California Innovations is offering $6 refunds for each large Cryofreeze gel pack and $5 for each of the other recalled packs. Image Credit: |More Lawsuit Stories Spinal Cord Stimulator Medical Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed May 29, 2026 Top Fitness Lawsuit Claims Home Gym Machine Failed, Crushing Womanโs Legs May 29, 2026 Midea Air Conditioner Recall Lawsuit Claims Window Unit Caused Severe Respiratory Illness May 29, 2026 0 Comments InstagramThis 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 Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: yesterday)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 2 days ago)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: 3 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)
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