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.
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
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.
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.
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.
Lean Pocket Recall: Plastic Found in Spinach Artichoke Chicken Pockets July 16, 2008 AboutLawsuits Add Your CommentsA “Lean Pocket” recall has been issued for nearly 200,000 pounds of frozen Spinach Artichoke Chicken sandwiches. It was discovered that some of the microwavable sandwiches produced on May 23, 2008, may contain small pieces of plastic. This could pose a risk of severe mouth, throat or intestinal injury.The recalled Lean Pockets were sold by the Nestle Prepared Foods Company, based in Mount Sterling, Kentucky. Lean Pockets are a low-calorie, stuffed sandwich, which are sold in various combinations of meats, cheese and vegetables within an enclosed crust. The recall only applies to Spinach Artichoke Chicken Lean Pockets, which are sold with two 4.5 oz. sandwiches in each package.All of the impacted Lean Pockets were produced on May 23, 2008 and sold nationwide at retail establishments after that date. The product packaging indicates: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 COMPENSATION“Lean Pockets Spinach Artichoke Chicken – 2 sandwiches”“Best Before” Date of “Nov 2009”Packaging Code starting with “8144544616”Establishment Number “P7721A”Nestle Prepared Foods Company did not discover the pieces of plastic in their Lean Pockets during quality checks, allowing the frozen sandwiches to be commercially sold. However, since the products were sold, they have received a number of customer complaints, including reports of at least two injuries suffered by consumers who ate the chicken pockets.In 2002, Nestle acquired Chef America, a pioneer in frozen, stuffed sandwiches, and established the Nestle Prepared Foods Company. The original sandwiches are still sold under the brand name “Hot Pockets” and consist of meats and cheese in a crust, which can be heated in a microwave. The Lean Pockets brand is a more recent low calorie version of the original sandwich and has a very low fat content.According to Nestle, the Lean Pocket recall only applies to the Spinach Artichoke Chicken variety of the sandwiches and not for any other “Lean Pocket” or “Hot Pocket” products. However, the manufacturer has not yet given any indication how the pieces of plastic were able to make their way into the sandwiches and how they can be sure that other products do not contain the same hazard.Consumers can contact Nestlรฉ Consumer Services Center at (800) 350-5016. Product liability lawyers recommend that any consumers who have been injured by pieces of plastic in their “Lean Pockets” should seek immediate medical attention and preserve any uneaten portion of the sandwich and packaging.UPDATE: On August 21, 2008, Nestle Prepared Foods, Inc. issued a Pepperoni Pizza Hot Pocket Recall for over 200,000 sandwiches which were also found to contain pieces of hard red plastic. Tags: Food Recall, Lean Pockets, Nestle, Product Liability Image Credit: Lean Pockets Recall|||More Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 4 Comments Elaine August 26, 2015 I am wondering when Lean Pockets Spinach Artichoke Chicken will be on the market again. I miss eating them. Frozen Chicken Recall: Small Pieces of Plastic in Stuffed Chicken Meals : AboutLawsuits.com January 21, 2009 […] issued on July 14, 2008, after the first consumer complaints, only included about 200,000 pounds of Lean Pocket Spinach Artichoke Chicken Sandwiches, subsequent recalls were issued on August 21, 2008, for 200,000 pounds of Hot Pockets Pepperoni […] Lean Cuisine Recall: Meals Could Be Contaminated with Pieces of Plastic : AboutLawsuits.com November 19, 2008 […] a result of reports that small pieces of hard plastic were in other types of their frozen foods. A Lean Pocket recall was issued in July 2008 and a Hot Pocket Pepperoni Pizza recall was issued in August 2008 for […] Hot Pocket Recall: Pieces of Plastic in Pepperoni Pizza Hot Pockets : AboutLawsuits.com August 25, 2008 […] PagesLean Pocket Recall: Plastic Found in Spinach Artichoke Chicken Pockets Filed Under: News • Recalls Tags: Hot Pockets • Lean Pockets • […] 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)