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February 13, 2024
Frigidaire Side-By-Side Refrigerator Choking and Laceration Lawsuit Lawyers
Electrolux Group has recalled Frigidaire side-by-side refrigerators with slim ice buckets made from 2015 to 2019 due to a defect in the ice bucket assembly that poses choking and laceration risks. This recall affects over 383,000 units in the U.S. and Canada. Consumers should check model numbers like DGHK2355TF and FGSC2335TF to see if their refrigerator is affected. Electrolux offers free replacements for the faulty component. Legal action is an option for those injured, with Parker Waichman LLP providing free consultations for affected individuals.
Frigidaire Refrigerator Recall: Choking Hazards & Legal Options for Affected Consumers
February 12, 2024
Dressing and Taco Kit Listeria Contamination Lawsuit Lawyers
A Listeria outbreak linked to Rizo-López Foods, Inc. has led to recalls of products from major retailers like Costco and Trader Joe's. Over 25 illnesses have been reported, prompting recalls of items like dressings and taco kits. Listeria poses serious health risks, especially to vulnerable groups. Affected individuals may seek legal compensation for damages through product liability lawsuits. Legal representation is crucial for navigating these complex cases, which can cover medical expenses, lost wages, and more. Parker Waichman LLP offers free consultations for those impacted.
Dressing and Taco Kit Listeria Outbreak: Legal Options for Affected Consumers
February 9, 2024
Philips BrightView SPECT Injury Lawsuit Lawyers
Philips has voluntarily recalled its BrightView SPECT nuclear imaging system due to potential safety risks, specifically the risk of detector movement caused by screw failure. This Class I recall, the most serious classification by the FDA, highlights the risk of serious injury or death. No injuries have been reported, but Philips is taking proactive measures, including inspections and safety notices. The recall affects about 1,000 systems worldwide. Healthcare providers are advised to avoid positioning patients' lower limbs under the detector to minimize risks. Philips remains committed to addressing safety issues with existing systems.
Philips BrightView SPECT Recall: Legal Options for Injury Victims and Patient Safety Concerns
February 9, 2024
CableMod Graphics Processing Unit Angled Adapter Fire Lawsuit Lawyers
CableMod's GPU V1.0 and V1.1 Angled Adapters have been recalled due to fire and burn hazards, affecting about 25,300 units. The adapters' male connectors can become loose, overheat, and melt into the GPU, posing significant safety risks. Victims of property damage from these defective adapters may seek legal recourse against CableMod Ltd. by consulting with a product liability attorney. Parker Waichman LLP offers free consultations to help victims pursue compensation for damages, including property damage and pain and suffering.
Understanding Legal Rights and Remedies for Victims Affected by Recalled CableMod GPU Angled Adapters
February 8, 2024
Atrium Express Dry Suction Dry Seal Chest Drain Lawsuit Lawyers
The FDA has issued a Class I recall for over 250,000 Atrium Express Dry Suction Dry Seal Chest Drains by Maquet Cardiovascular due to sterility concerns with the water syringe, posing risks of serious infections. These devices, used post-cardiothoracic surgery, could lead to severe health issues if contaminated. Affected patients may file lawsuits for damages. Legal assistance is advised to navigate the complexities of product liability claims. Parker Waichman LLP offers free consultations for those impacted by these defective chest drains.
FDA Issues Urgent Recall of 250,000 Atrium Express Chest Drains Due to Serious Safety Risks
February 8, 2024
SRAM LLC Bicycle Shift Brake Lever Injury Lawsuit Lawyers
SRAM LLC has issued a voluntary recall of certain shift brake levers due to a potential crash hazard, in collaboration with the U.S. Consumer Product Safety Commission. The recall affects models like SRAM Apex AXS and Red eTap AXS, sold from June 2019 to October 2023. The clamp bolt on these levers may loosen, risking rider safety. Consumers should stop using the levers and contact SRAM for a free inspection. Legal recourse may be available for those injured due to the defect.
SRAM LLC Brake Lever Recall: Protecting Cyclists from Crash Hazards - Legal Options for Injured Riders
February 8, 2024
Rizo Brothers California Creamery Listeria Monocytogenes Lawsuit Lawyers
Rizo-Lopez Foods, Inc., known as Rizo Brothers California Creamery, has voluntarily recalled various dairy products due to potential Listeria contamination. The recall, advised by the CDC and FDA, affects products distributed nationwide through retailers like El Super and Cardenas Market. Listeria monocytogenes can cause severe illness, especially in vulnerable groups. Consumers should discard affected products and may contact the company for guidance. Legal action may be pursued by those harmed, with firms like Parker Waichman LLP offering support for product liability claims.
Rizo Brothers California Creamery Dairy Products Recall: Listeria Monocytogenes Risk and Legal Options
February 8, 2024
New York Bill Makes it Easier for PFAS Victims in New York to Sue Manufacturers for Damages
New York is addressing chemical pollution, particularly from PFAS, known as "forever chemicals," used in products like non-stick cookware and water-repellent clothing. These chemicals are linked to health issues such as cancer and thyroid problems. The PFAS Accountability Act, led by Senator Kirsten Gillibrand, aims to hold manufacturers accountable and ensure long-term medical monitoring for affected individuals. Victims face legal challenges in proving their cases, but successful lawsuits can result in compensation for medical expenses and other damages. Parker Waichman LLP offers free consultations to help victims seek justice.
PFAS Lawsuits in New York: Understanding Your Legal Rights and Seeking Justice for Chemical Exposure
February 8, 2024
Fisher-Price Infant-to-Toddler Rocker Suffocation Wrongful Death Lawsuit Lawyers
Consumer Reports has raised concerns about the safety of Fisher-Price baby rockers following the death of a 6-month-old in November 2023. They urge Mattel, the parent company, to recall these products. This incident highlights ongoing safety issues, as previous warnings were issued after multiple infant deaths linked to these rockers. Consumer Reports advises parents to avoid using inclined products for infant sleep. Legal action is suggested for affected families, emphasizing the need for accountability and safer product designs.
Fisher-Price Infant to Toddler Rocker Safety Concerns: Urgent Recall Request & Legal Options for Victims
February 7, 2024
Recalled Philips CPAP and BiPAP Machines Linked to Over 560 Deaths
The FDA has updated a recall of Philips sleep apnea machines, linking them to at least 561 deaths. The recall involves BiPAP and CPAP devices, which may release harmful particles due to degrading foam. This poses serious health risks, including cancer. Philips recalled over 5 million devices in 2021 and stopped U.S. sales. Affected individuals can pursue lawsuits for damages. Legal assistance is crucial for navigating these complex cases and seeking compensation for injuries or wrongful death. Parker Waichman LLP offers free consultations for those impacted.
Philips Sleep Apnea Machines Recall: Health Risks, Lawsuits & Safety Concerns Explained
February 7, 2024
iFIT NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbell Injury Lawsuit Lawyers
iFIT has recalled its NordicTrack 50 LB iSelect Voice-Controlled Adjustable Dumbbells due to an impact hazard, affecting about 15,400 units in the U.S. and 650 in Canada. The recall, announced on February 1, 2024, is due to weight plates potentially dislodging during use, posing a risk of injury. There have been 40 incidents reported, with eight resulting in injuries. iFIT advises users to stop using the dumbbells and contact them for a refund. Legal options are available for those injured, with Parker Waichman LLP offering free consultations.
iFIT Recalls NordicTrack 50 LB iSelect Dumbbells: Important Safety Warning and Legal Options
February 7, 2024
FDA Cautions Consumers About Potentially Contaminated and Ineffective Eye Drops
The FDA has issued a warning about South Moon, Rebright, and FivFivGo eye drops due to contamination and ineffectiveness concerns. These unapproved products mimic Bausch + Lomb's Lumify eye drops. Testing revealed South Moon's contamination with Burkholderia cepacia complex, a bacteria that can cause antibiotic-resistant infections. Rebright tested negative, and FivFivGo wasn't tested. The FDA advises against using these products, noting the absence of the active ingredient brimonidine tartrate. Consumers should dispose of these eye drops and report any adverse effects to the FDA's MedWatch program.
Contaminated Eye Drops: Understand Risks and How to File a Lawsuit for Compensation
February 5, 2024
Robitussin Cough Syrup Microbial Contamination Lawsuit Lawyers
Robitussin cough syrups have been recalled nationwide due to potential microbial contamination, affecting eight lots of Robitussin Honey CF Max Day and Nighttime Adult syrups. The recall, initiated by Haleon, targets products with expiration dates through 2025 and 2026. While no adverse events have been reported, the recall is particularly concerning for immunocompromised individuals due to risks of severe infections. Consumers are advised to stop using the products and return them. Legal options may be available for those affected, with Parker Waichman LLP offering free consultations for potential product liability claims.
Robitussin Cough Syrup Recall: Legal Guidance for Affected Consumers and Potential Lawsuits
February 5, 2024
Philips Suspends Sales of Breathing Machines in the U.S. After Major Recall
Philips Respironics has halted U.S. sales of its breathing machines after settling with the FDA over issues with CPAP and ventilator devices. Reports indicated these devices emitted harmful particles and gases, raising safety concerns. Philips must revamp its operations before resuming sales. The recall began in June 2021 due to potential health risks. Despite Philips' claims of safety, the FDA remained skeptical, prompting further recalls. Affected individuals may seek legal action for injuries through product liability lawsuits, with legal guidance recommended for navigating the process.
Philips Halts Sales of Breathing Machines: What You Need to Know About Device Safety and Legal Options
February 5, 2024
FDA Issues Warning on CAR-T Therapy Cancer Risk
The FDA has issued a warning about CAR-T therapies, which are linked to secondary blood cancers. Companies must now include boxed warnings on these products and monitor patients for such cancers. Despite these concerns, the benefits of CAR-T therapy, especially for patients with limited options, are considered to outweigh the risks. The FDA's actions aim to ensure patient safety while maintaining the potential of CAR-T therapies. Legal options are available for those harmed by these treatments, with firms like Parker Waichman LLP offering consultations for affected individuals.
FDA Warning: CAR-T Therapy Linked to Secondary Cancer Risks - What You Need to Know
February 4, 2024
Snap Initiates Massive Recall of 71,000 Drones Due to Fire Hazard
Snap has recalled 71,000 Pixy drones due to safety concerns with their lithium-ion batteries, which have caused overheating and bulging, leading to a minor fire and one injury. The drones, priced between $185 and $230, were introduced in 2022 but discontinued after four months. Snap offers full refunds and advises safe battery disposal. The recall highlights broader issues with lithium-ion batteries, which have caused numerous fires. Victims of such incidents may seek compensation through product liability lawsuits, with legal assistance available from firms like Parker Waichman LLP.
Snap Drone Fire Hazard: Lawsuits Filed After 71,000 Pixy Drones Recalled for Battery Issues
February 2, 2024
Fat-Dissolving Injection Injury Lawsuit Attorneys
The FDA has issued a warning about the dangers of unapproved fat-dissolving injections, such as Aqualyx and Lipodissolve, which contain phosphatidylcholine (PPC) and sodium deoxycholate (DC). These injections have not been evaluated for safety and effectiveness, leading to reports of adverse reactions like permanent scars and infections. The only FDA-approved fat-dissolving injection is Kybella, intended for use under the chin. Consumers are advised to consult healthcare professionals and avoid unapproved products. Legal action may be pursued for injuries caused by these injections.
FDA Issues Warning: The Risks of Unapproved Fat-Dissolving Injections Containing Phosphatidylcholine and Sodium Deoxycholate
February 2, 2024
Byrne Dairy Mighty Fine Chocolate Ice Cream Peanut Allergy Lawsuit Lawyers
Byrne Dairy, Inc. has recalled its Mighty Fine Chocolate Ice Cream due to undeclared peanuts, posing risks to those with peanut allergies. The FDA warned consumers about the potential dangers, as the affected half-gallon cartons were sold in Upstate New York. No illnesses have been reported, and the recall involves no more than 250 units. The mislabeling resulted from a manufacturing error. Consumers should not consume the product and can return it for a refund. Legal options are available for those affected by such defective products.
Ice Cream Recall: Byrne Dairy Warns of Life-Threatening Peanut Allergy Risks
February 2, 2024
Philips and FDA Reach Agreement Concerning Philips Sleep Apnea Machines
Philips, a Dutch health technology company, faces a major setback in the U.S. due to a halt in sales of new sleep apnea devices. This follows a 2021 recall over toxic foam concerns, leading to a consent decree with the FDA requiring improvements at U.S. facilities. Philips' shares fell 8.3% after the announcement, while rival ResMed's shares rose. The decree's finalization is pending court approval, and Philips has set aside 363 million euros for related costs. The company also faces lawsuits and a U.S. Department of Justice investigation.
Philips Sleep Apnea Machines: FDA Consent Decree Halts Sales Amid Health Risks and Lawsuits
February 1, 2024
FDA Discovers Manufacturing Failures Behind Applesauce Lead Poisoning Recall
The FDA has recalled cinnamon-flavored applesauce pouches made by Austrofood S.A.S in Ecuador due to lead contamination. The recall follows an inspection revealing inadequate quality control and lack of heavy metal testing. The contaminated products have been linked to 385 lead poisoning cases across 42 U.S. states, primarily affecting children. The FDA found high lead levels in the products and noted deficiencies in manufacturing processes. Legal action is suggested for affected individuals, with Parker Waichman LLP offering free consultations for potential product liability lawsuits.
Applesauce Lead Poisoning Recall: FDA Reveals Serious Quality Control Failures in Cinnamon Pouches
January 30, 2024
Off-Highway Vehicle (OHV) Accidents Are on The Rise
In 2023, the Consumer Federation of America reported 498 fatalities related to off-highway vehicles (OHVs), highlighting significant risks, especially for children under 15, who made up 19% of these deaths. Dr. Gary Smith emphasized that children under 16 are not equipped to safely operate OHVs. A concerning 67% of fatalities occurred on roads, despite OHVs not being designed for such use. The CFA advocates for safety measures, including avoiding road use, wearing protective gear, and ensuring children do not ride adult-size OHVs. They also provide resources like an ATV safety toolkit for parents.
Off-Highway Vehicle Accident Statistics 2023: Alarming Insights into Fatalities and Child Safety Risks
January 30, 2024
Ingenuity Dream & Grow Bedside Bassinet Suffocation Death Lawsuit Lawyers
Concerns have been raised about the safety of two baby bassinets, the Ingenuity Dream & Grow Bedside Bassinet and the Halo BassiNest Flex Portable Bassinet, due to their tendency not to remain level. This instability can cause infants to roll into dangerous positions, posing a suffocation risk. The Consumer Product Safety Commission (CPSC) has documented infant deaths related to similar bassinets. Consumer Reports confirmed these safety issues, and a class-action lawsuit has been filed against Halo Innovators. Parents are advised to report incidents and seek legal advice if necessary.
Ingenuity Dream & Grow Bedside Bassinet Lawsuits: Safety Concerns & Parent Warnings
January 30, 2024
Yaomiao Tiaras Lead Poisoning Lawsuit Lawyers
Children's safety is crucial, especially with products designed for them. Recently, children's tiaras sold on Amazon under the "Yaomiao" brand were recalled due to excessive lead content, posing health risks. Over 12,000 sets sold between January 2021 and November 2023 are affected. The Consumer Product Safety Commission advises discarding these tiaras immediately. Buyers can receive refunds. Legal action may be necessary for those affected, and Parker Waichman LLP offers free consultations for potential product liability lawsuits to ensure justice and compensation for victims.
Yaomiao Tiaras Lead Poisoning Recall: Important Information for Parents and Legal Help
January 27, 2024
UK Identifies Cancer-Causing Chemicals in U.S. Food Products
In the UK, sweets imported from the US, such as Jolly Ranchers and Swedish Fish, have been found to contain illegal, carcinogenic ingredients banned by the UK government. These candies, popular on social media, include harmful substances like mineral oil and Calcium Disodium EDTA. Trading standards officers have seized thousands of pounds worth of these sweets from shops. Despite being legally produced in the US, these products are sold illegally in the UK. The rise in imports highlights the growing presence of these banned items in the market.
Cancer-Causing Chemicals Found in Popular US Sweets: What Parents Need to Know
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