Our Posts

New York City, known for its vibrant pedestrian life, faces a significant challenge in ensuring pedestrian safety due to frequent right of way violations. Despite clear laws requiring drivers to yield to pedestrians, especially at intersections and crosswalks, these rules are often ignored, leading to numerous accidents and injuries. Establishing liability in such cases involves gathering evidence like surveillance footage and eyewitness accounts. Injured pedestrians have the right to seek compensation for medical expenses and emotional distress. Preventive measures and community advocacy are crucial in promoting pedestrian safety and reducing accidents.

The Consumer Product Safety Commission (CPSC) has expressed concerns over infant deaths linked to nursing pillows, particularly when used during sleep. These u-shaped pillows, popular among breastfeeding mothers, have been associated with 171 infant deaths between 2004 and 2015. The CPSC advises against using pillows with infants, emphasizing safe sleep practices. Despite concerns from the Breastfeeding Infant Development Support Alliance about potential impacts on breastfeeding, the CPSC aims to implement guidelines to prevent suffocation risks without banning the pillows entirely.

Sensio has recalled several pressure cooker models due to safety concerns after 61 burn injuries were reported. The issue involves the lid unlocking prematurely, causing hot contents to spill. Affected models include electric and stovetop versions from brands like Bella, Bella Pro Series, Crux, and Cooks. Consumers are advised to stop using these cookers and seek refunds. The products were sold at major retailers from 2015 to 2020. Injuries reported include second- and third-degree burns, with risks of scalding, eye injuries, and property damage.

A recent tragedy in New York City has heightened concerns over e-bike safety after a fire, believed to be caused by a faulty e-bike battery, resulted in the death of a 93-year-old woman. This incident is part of a growing number of fatalities linked to defective e-bike batteries, with over 100 battery-related fires reported in the city this year, causing at least 14 deaths. The risks associated with lithium-ion batteries, such as manufacturing defects and overcharging, underscore the need for improved safety measures and consumer awareness.

Gary Flook dedicated 37 years to the Air Force as a firefighter, using aqueous film forming foam (AFFF) at bases in Illinois and Indiana. Unaware of its hazards, he was diagnosed with testicular cancer in 2000, linked to PFAS chemicals in the foam. Recent studies confirm a connection between PFAS and cancer in military personnel. Despite awareness, the Department of Defense still uses these foams, facing criticism and lawsuits. Flook is among those suing manufacturers for health impacts, highlighting the need for safer alternatives and broader awareness.

Philips Respironics has recalled several ventilator models, including Trilogy Evo and Trilogy Evo O2, due to contamination risks that may obstruct airflow, potentially causing serious injury or death. The FDA classified this as a Class I recall, the most severe type. The recall affects 73,000 devices distributed in the U.S. from March 2019 to March 2023. Philips advises using approved filters and having backup ventilation. Patients and caregivers using these devices should be vigilant and report any issues to the FDA's MedWatch Program.

A Columbus-based family was awarded $787 million in a wrongful death case after their 2-year-old son died from positional asphyxiation while playing on a bunk bed purchased from Wayfair. The bed, made by Moash Enterprise Company Limited, had a design flaw that led to the tragedy. Despite a recall in December 2022, the bed remained available online. The family's attorney highlighted the safety issues, and the jury's verdict is one of the largest in state history.

The article discusses the disparities between the World Trade Center Health Program and the September 11 Victim Compensation Fund, highlighting how a new law, the "9/11 Notice Act," aims to address these issues. The law mandates that employers near Ground Zero during the attacks notify employees about potential health risks and compensation eligibility. Despite available funds, many survivors remain unaware of their entitlements, unlike first responders who have better access to these programs. The legislation seeks to improve awareness and support for civilians affected by 9/11-related health issues.

Gree, a leading consumer electronics company, has recalled 1.56 million dehumidifiers due to fire and burn hazards. These devices, sold under various brand names like Kenmore and GE, can overheat and catch fire, with at least 23 fires reported, causing $168,000 in property damage. Manufactured between 2011 and 2014, the affected models should be unplugged immediately. Consumers are urged to contact Gree for a refund. The dehumidifiers were sold at major retailers, including Home Depot and Walmart, with prices ranging from $110 to $400.

On August 14, 2023, Polaris Industries Inc. recalled 2021 RZR XP Turbo and Turbo S off-road vehicles due to fire and injury hazards from a clutch defect. This recall affects about 27,300 units in the U.S. and 660 in Canada. Owners are advised to stop using the vehicles and contact Polaris for a free clutch replacement. The recall follows reports of clutch failures, including fires and injuries. Affected owners should verify their vehicle's VIN on the Polaris website and follow repair instructions. Legal action may be considered for those harmed.

Daimler Trucks North America (DTNA) has recalled 1,280 units of 2023 models, including Freightliner, FCCC, and Thomas Built vehicles, due to potential driveshaft failures. The recall, identified by NHTSA campaign number 23V537000, addresses the risk of driveshafts breaking under certain conditions, which could lead to loss of drive power and increased crash risk. DTNA will replace the affected driveshafts free of charge, with owner notifications starting September 30, 2023. Owners should contact DTNA customer service or the NHTSA for more information.

Restwell Mattress Co. has recalled two crib mattress models sold at Room & Board due to non-compliance with federal safety standards, posing a suffocation risk to infants. The recall affects approximately 100 units sold between August 2022 and June 2023. Customers should stop using the mattresses immediately and contact Room & Board for a free pickup and refund. No injuries have been reported. For more information, customers can visit the Restwell Mattress or Room & Board recall pages or contact Room & Board directly.

Philips Personal Health has recalled approximately 12,850 Philips Avent Digital Video Baby Monitors due to a burn hazard from overheating lithium-ion batteries in the Parent Unit. The recall, announced on August 3, 2023, affects models SCD630 and SCD843, manufactured between March 2016 and December 2019. No incidents have been reported in the U.S., but 23 overheating cases and seven minor injuries occurred in Europe. Consumers should stop using the monitors and contact Philips for a free replacement. More information is available on Philips' website or by calling their toll-free number.

The U.S. Consumer Product Safety Commission has unanimously voted to enforce regulations banning inclined sleepers for infants and crib bumpers, as mandated by the Safe Sleep for Babies Act. These regulations, effective since November 12, 2022, prohibit the manufacture, sale, distribution, and importation of these products in the U.S. The rules aim to enhance infant safety by defining inclined sleepers as those with a sleeping surface angled over ten degrees and banning crib bumpers designed to prevent harm from crib sides, excluding non-padded mesh liners.

The U.S. Consumer Product Safety Commission (CPSC) has issued a warning about La-La-Me infant loungers, urging consumers to stop using them due to significant suffocation and fall risks. These loungers, sold online and priced between $60 and $130, fail to meet federal safety standards. Despite the hazards, La-La-Me has not agreed to a recall. The CPSC advises cutting and disposing of the loungers and reporting any incidents. Parents are reminded to follow safe sleep guidelines for infants. The CPSC continues to protect consumers from unsafe products.

Truck accidents in New York State often result in severe injuries and fatalities, making it crucial to prove negligence for victims seeking justice. This guide outlines the key elements of negligence—duty of care, breach of duty, causation, and damages—and the unique challenges in truck accident cases, such as federal regulations and multiple parties involved. Gathering evidence, utilizing expert witnesses, and building a compelling case are essential steps. Legal representation is vital in navigating these complexities to secure rightful compensation for victims. Parker Waichman LLP offers free consultations for affected families.

The FDA has issued a Class I recall for Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps due to a defect causing unexpected shutdowns, posing life-threatening risks. Manufactured by Datascope/Maquet/Getinge, these devices support the heart's left ventricle. The recall affects over 4,500 devices in the U.S. Healthcare providers and patients using these pumps are at risk. The manufacturer has advised ensuring alternative support is available. Legal action may be necessary for those affected, with guidance available from Parker Waichman LLP for compensation claims.

In Norfolk, Virginia, Jessica Gurley purchased a Bedsure Electric Blanket from a discount store, only to discover it had been recalled due to fire and burn risks. This incident highlights the dangers of buying secondhand items without checking for recalls. Consumers are urged to verify product safety through resources like cpsc.gov and to be cautious with resale items. Gurley's experience serves as a reminder of the potential risks associated with secondhand purchases and the importance of consumer vigilance.

A tuberculosis outbreak in the U.S. has been linked to contaminated bone graft materials, marking the second such incident in two years. The outbreak resulted in one death and infected at least four others. Aziyo Biologics, the company involved, recalled the affected products after they were used in surgeries and dental procedures. The CDC reported that 36 patients received the contaminated grafts. Current regulations do not require TB testing for tissue donors, prompting calls for more stringent testing and regulations to prevent future outbreaks.

Abbott has issued a Class I recall for its Amplatzer Steerable Delivery Sheath, model ASDS-14F-075, due to a risk of air embolism, which can cause severe health issues such as stroke or death. The recall affects 672 devices distributed in the U.S. between October 2022 and February 2023. Abbott has reported 26 incidents and 16 injuries related to this issue. Affected customers are advised to return unused devices and use alternative systems. Abbott emphasizes patient safety and regulatory compliance in addressing this issue.

GE HealthCare has recalled 7,559 TruSignal SpO2 Sensors in the U.S. due to serious safety concerns. The recall, initiated on May 19, 2023, involves malfunctioning sensors that may reduce defibrillation energy, expose patients to unintended electrical currents, and provide inaccurate SpO2 readings. These issues pose significant risks, including potential injuries or death. GE HealthCare advises using alternative monitoring methods and following specific guidelines if using affected sensors. The FDA classified this as a Class I recall, the most serious type, although no injuries have been reported.

The FDA has announced a Class I recall of nearly 8,000 Impella blood pumps by Abiomed due to potential harm or fatality risks for patients with prior transcatheter aortic valve replacement (TAVR). The recall aims to improve consumer awareness, as the pumps may cause serious injuries or death if used improperly. The affected models include Impella 5.0, CP, 2.5, CP with SmartAssist, LD, and 5.5 with SmartAssist. There have been 30 incident reports, including 26 injuries and four deaths. Legal action may follow for those affected.

The Bard PowerPort, an implantable port catheter system, has faced numerous reports of complications since its FDA approval in 2000. Issues include catheter fractures and migrations, leading to severe infections and other injuries. Legal actions allege design flaws and inadequate risk disclosure by the manufacturers, Becton Dickinson & Company and its subsidiaries. Despite these allegations, no recall has been issued. Those affected may be eligible for compensation and are advised to consult specialized lawyers. Parker Waichman LLP offers legal assistance on a contingency fee basis for such cases.

The FDA has announced a Class I recall of nearly 8,000 Impella blood pumps by Abiomed due to potential harm or fatality risks for patients who have undergone transcatheter aortic valve replacement (TAVR). The recall affects several Impella models shipped since May 2021. The devices may cause serious injuries or death if the pump's motor interacts with the TAVR valve, potentially leading to reduced blood flow or pump failure. There have been 30 incident reports, including 26 injuries and four deaths. Legal actions may follow for affected individuals.