MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking
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 Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
Jonathans Alfalfa Sprout Recall Expanded to Organic Sprouts April 26, 2011 AboutLawsuits Add Your CommentsAn alfalfa sprout recall initially issued last week for some Jonathan’s Sprouts products due to a risk of salmonella contamination is now being expanded to encompass additional lots and some of the company’s organically grown sprouts as well. The Jonathan’s Sprouts recall expansion was announced on April 22 by the FDA, adding all sell-by dates for the affected products as well as 4-oz packages of Jonathan’s Organic Sprouts and Jonathan’s Organic Sprout Salad. Originally, none of the products affected by the original recall were organic and the recall was restricted to products with sell-by dates of April 23.The recall now affects 4oz packages of Jonathan’s Alfalfa Sprouts, Alfalfa with Radish Sprouts, Gourmet Sprouts, Alfalfa with Dill Sprouts, Organic Alfalfa Sprouts, and 8 oz packages of Alfalfa Sprouts. It also affects packages of Jonathan’s Organic Sprout Salad; all sell-by dates are affected.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 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 COMPENSATIONAlso included in the recall are Jonathan’s 5 lbs. Bulk Alfalfa in waxed 18” x 11” cardboard cartons – all codes; 5 lbs. Bulk Organic Alfalfa in waxed 18” x 11” cardboard cartons – all codes; and 4lb Bulk Alfalfa Sprouts in 2lb bags in a 13”x9”x6” cardboard carton – all codes.The recalled sprouts were sold at A&P, Grand Union, Stop & Shop, Shaws, Hannaford, Donnelans, Foodmaster, Truccis, and Roche Brothers stores in Maine, New Hampshire, Vermont, Massachusetts, Rhode Island, Connecticut, New York, Maryland, New Jersey, Pennsylvania, and Delaware. The salmonella contamination was discovered by the USDA Microbiological Data Program.The FDA recently issued a warning letter to Jonathan’s Sprouts Inc. regarding claims it was making about the health benefits associated with its sprouts. According to the FDA, the Rochester, Massachusetts-based company promoted many of its products as cancer-fighting agents and as being capable of lowering cholesterol. Federal regulations limit the health benefit and nutrition claims that can be made about foods to those that have been authorized by regulation. To make such claims, the FDA told the company that its sprouts would have to qualify as a new drug and be treated accordingly.Salmonella is a type of bacteria that attacks the gastrointestinal tract, causing mild to severe food poisoning. For most healthy adults, symptoms of food poisoning from salmonella typically resolve after a few days or weeks. However, young children, the elderly, and individuals with compromised immune systems have an increased risk of suffering severe food poisoning after ingesting the bacteria. If not properly treated, some cases of salmonella food poisoning can lead to hospitalization, dehydration or death.Any consumers who have purchased sprouts affected by the recall should return them to the place of purchase for a full refund. Any consumers with questions can contact the company at 508-763-2577. Tags: Alfalfa Sprout, Alfalfa Sprout Recall, Connecticut, Delaware, Food Poisoning, Maine, Maryland, Massachusetts, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Salmonella, Salmonella Food Poisoning, Vermont Image Credit: |More Lawsuit Stories Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials August 12, 2026 MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026 Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026 0 Comments CompanyThis 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 Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: today)C.R. 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Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials August 12, 2026
MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026
Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026
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