Our Posts

Ashley Furniture Industries has recalled its Party Time Collection Loveseats, Sofas, and Recliners due to a fire hazard from overheating LED cupholders. Announced on June 8, 2023, the recall affects about 253,000 units in the U.S. and 9,450 in Canada. No injuries have been reported, but six incidents of overheating have occurred. Consumers should unplug the units and contact Ashley Furniture for a free repair. The products were sold from November 2018 to March 2023, priced between $900 and $1,800.

T.W. Garner Food Company is recalling 50,688 bottles of Texas Pete® Buffalo Wing Sauce due to a labeling error where some bottles may contain Texas Pete® Extra Mild Wing Sauce, which includes soy. This poses a risk to individuals with soy allergies. The affected bottles have a best-use-by date of 120623T 065239 and UPC 0 75500 10011 6. No illnesses have been reported. Consumers with soy allergies should not consume the product and can return it for a refund. The product was distributed in several U.S. states.

Pre-made meals from supermarkets offer convenience similar to sliced bread in the 1920s, but they come with potential drawbacks. Studies have linked these meals to obesity, and concerns exist about ingredient freshness, undeclared allergens, and discrepancies in labeling. Pre-made meals may also contain higher levels of salt and saturated fat than expected, posing health risks. Additionally, there is a risk of foodborne contaminants and potential plastic contamination when microwaving in plastic containers. Consumers should be cautious and informed when purchasing and consuming these meals.

The U.S. Consumer Product Safety Commission and The Boppy Company have urged consumers to stop using recalled Boppy Newborn Loungers due to suffocation risks. Despite a 2021 recall, two more infant deaths have occurred. The loungers remain illegal to sell, and online platforms are asked to remove them. Consumers should contact Boppy for disposal instructions and refunds. Legal action may be pursued for harm caused by these products, with potential compensation for medical expenses and other damages. Parker Waichman LLP offers free consultations for affected families.

The FDA warns against the ingestion or inhalation of nitrite "poppers," which can cause severe health issues, including death. These products, often sold as air fresheners or deodorizers, mimic amyl nitrite but are not FDA-approved. They can cause skin damage, breathing difficulties, and heart problems. Misleading packaging may resemble energy shots, increasing the risk of accidental misuse. Consumers are urged to avoid these products and report adverse effects to the FDA. Legal action may be pursued for injuries caused by poppers, with guidance from a personal injury attorney.

The FDA reported that Philips ventilators, BiPAP, and CPAP machines, part of a recall, may have caused 40 more deaths, raising the total to 385 since June 2021. Over five million devices are under repair due to foam degradation. From January to March, the FDA received over 6,000 reports, adding to more than 105,000 since April 2021. Philips claims most reports indicate technical issues without serious injury. The recall is classified as "Class I," suggesting potential severe health risks. Philips plans to cut 10,000 jobs by 2025 to improve operations.

Novis PR LLC has recalled a batch of G-Supress DX Pediatric Drops due to mislabeling, where the product was found to contain Finafta Anesthetic/Analgesic Liquid instead of the intended cough suppressant. This liquid, not produced by Novis, contains 60% ethyl alcohol and 5% benzocaine, posing serious health risks to children, including alcohol toxicity and methemoglobinemia. The FDA advises against purchasing Lot# D20911, distributed only in Puerto Rico. No adverse events have been reported, and customers can contact Novis for inquiries.

Strokes are critical medical emergencies requiring immediate diagnosis and treatment. Misdiagnosis in emergency rooms can lead to severe consequences, including permanent disability or death. A recent study highlights that 1 in 18 emergency room patients are misdiagnosed, with 2.6 million experiencing preventable harm. Misdiagnosis can occur due to lack of awareness, diagnostic errors, or communication breakdowns. Legal action may be pursued in such cases, emphasizing the need for improved diagnostic practices and patient safety. Parker Waichman LLP offers legal assistance for those affected by emergency room stroke misdiagnosis.

An 18-year-old baseball player from Central Penn College died after being injured by the collapse of an illegally constructed dugout in Harrisburg. The incident occurred during the dismantling of the dugout, which was ordered by city officials. The player was struck in the face, suffered severe injuries, and was taken to the hospital in critical condition. The community mourns his loss, offering support to his family, friends, and teammates. The tragedy highlights the importance of safety and accountability in construction practices.

The FDA has announced a recall of 466 units of Abiomed's Impella 5.5 with SmartAssist heart pumps due to a risk of purge fluid leakage, which can lead to serious injuries or death. The recall, classified as Class I, follows 179 complaints and three reported injuries. Affected customers are advised to stop using the devices unless no alternatives are available and to contact Abiomed for returns. Legal actions, including wrongful death lawsuits, may arise from the defects. The latest Impella models with updated features are not affected by this recall.

The New York Senate approved a proposal to extend workers' compensation benefits for mental stress to all employees experiencing extreme stress, following a similar proposal's veto by Governor Kathy Hochul in 2022. The bill, A.B. 5745, passed with a 40-18 vote and moves to the state Assembly. It aims to broaden employer responsibility for mental distress by removing current restrictions that limit benefits to specific roles like emergency responders. The law would cover all employees facing exceptional work-related stress, with implementation set for the following year.

Ford, in collaboration with the National Highway Traffic Safety Administration, has issued a warning to owners of about 143,000 Lincoln MKC SUVs from 2015 to 2019 due to a fire risk. The issue stems from a battery monitoring sensor that could short circuit and cause a fire. Owners are advised to park their vehicles outdoors and away from other cars. Ford will install a fuse at no cost to prevent this risk. Instructions will be mailed to owners, and they can contact Lincoln dealerships or Ford customer service for more information.

Motor vehicle traffic crashes in New York State from 2012-2014 resulted in an average of 1,098 deaths, 12,093 hospitalizations, and 136,913 emergency department visits annually. Males and those aged 65 and older had the highest fatality rates. Death rates decreased from 8.4 per 100,000 in 2001 to 4.9 in 2014. Hospitalization rates also declined from 87.5 per 100,000 in 2002 to 57.0 in 2014. Emergency visits averaged 696.6 per 100,000, with a general decrease over the years. Prioritizing road safety is essential to reduce these incidents.

Shaquille O’Neal is facing a lawsuit for alleged securities violations related to his NFT collection, Astrals. The lawsuit, filed by Daniel Harper in Florida, claims O’Neal breached the Securities Act of 1933 by selling unregistered securities. Harper, who bought 96 Astrals NFTs, suffered losses after the crypto market downturn. The case may apply the Howey test to determine if Astrals are securities. O’Neal promoted the NFTs with potential investment returns, and the lawsuit reflects broader legal scrutiny of NFTs as securities.

A study by the National Institutes of Health found a link between regular use of certain hair products, like chemical straighteners, and an increased risk of uterine cancer. This has led to lawsuits against companies like L’Oréal, with claims that these products contributed to health issues such as endometriosis. The study noted that black women are the primary users of these products. Despite the findings, uterine cancer remains rare, and the study did not conclusively prove causation. Legal actions are being pursued by affected individuals seeking compensation.

The Consumer Product Safety Commission (CPSC) is considering updating federal bicycle regulations to enhance e-bike safety, inviting public input over the next 60 days. This move comes as e-bike usage rises, bringing safety concerns such as injuries and fires. The CPSC aims to assess current guidelines' applicability to e-bikes and address issues like unsafe batteries. Public feedback will help shape potential new regulations. Organizations like PeopleForBikes support these efforts, emphasizing the need for robust safety standards. The CPSC also seeks opinions on specific children's bike regulations.

In September 2021, the Consumer Product Safety Commission (CPSC) warned against using the Boppy Newborn Lounger after it was linked to infant deaths. Despite this, regulatory actions were limited, and baby loungers remain available, leading to further fatalities. Families affected by these tragedies are pursuing lawsuits against manufacturers, seeking accountability and stricter regulations. These legal actions aim to highlight the dangers of baby loungers and push for comprehensive safety standards. Meanwhile, some states are considering bans to address the immediate risks posed by these products.

Tesla is recalling 137 Model Y vehicles due to a potential steering wheel detachment issue, identified by a service technician. The problem is linked to a single fastener that may not be properly tightened, affecting about 10% of the recalled vehicles. Tesla has acknowledged four warranty claims and one field report related to this issue but reported no accidents or injuries. This recall follows previous incidents and an NHTSA investigation. The defect could lead to product liability lawsuits if it results in accidents or injuries.

Tepezza, an FDA-approved injection for thyroid eye disease (TED), is facing scrutiny due to studies linking it to irreversible hearing damage and tinnitus in some patients. Despite initial claims by Horizon Therapeutics that hearing issues were temporary and affected only 10% of users, research indicates a higher risk. Lawsuits allege inadequate warnings about these risks. Patients experiencing hearing loss after Tepezza treatments may qualify for legal action and compensation. Legal firms are actively accepting cases related to hearing impairment caused by Tepezza.

A news report from MedPageToday.com highlights the growing incidence of breast implant-associated anaplastic large-cell lymphoma (BIA-ALCL). As of late 2022, 1,333 global cases and 35 deaths were reported, with 402 cases and eight deaths in the U.S. BIA-ALCL is linked to textured implants, not smooth ones. The FDA has noted additional risks, including squamous-cell carcinoma and B-cell lymphoma. Treatment primarily involves surgery. Legal action for affected individuals may involve product liability claims against manufacturers for design, manufacturing, or marketing defects.

Avanos Medical Inc. has recalled 1,000 BALLARD ACCESS Closed Suction Systems for Neonates/Pediatrics due to cracked manifolds, posing risks of inadequate ventilation and serious harm. The FDA classified this as a Class I recall, the most severe type. Distributed between October 2022 and January 2023, the recall began in February 2023. Affected devices include those with Y-Manifold and Elbow Manifold. Cracked manifolds can lead to respiratory circuit leaks, risking brain damage or death. Parents may consider wrongful death lawsuits, requiring legal consultation and evidence collection.

On May 23, 2023, U.S. health authorities warned about a recall of eye drops linked to four deaths and numerous injuries due to contamination with antibiotic-resistant Pseudomonas aeruginosa. Over ten brands, including Global Pharma's EzriCare and Delsam Pharma, were recalled. Despite the February recall, these products continue to pose health risks. The CDC reported 81 infections across 18 states. Users are urged to stop using these products and seek medical advice. Legal options are available for those affected.

Uterine cancer is now covered for 9/11 responders and survivors under the World Trade Center Health Program, providing free treatment and inclusion in the September 11 Victims Compensation Fund. Previously excluded, this decision offers relief to many, though it came too late for some, like Kataryzna Sosnowski, who died from the disease. The inclusion process began in 2021, acknowledging the potential link between 9/11 exposure and uterine cancer. This change aims to improve awareness and access to preventive screenings for affected women.

Contaminated eye drops have been linked to four deaths and 14 cases of vision loss, according to the CDC. The outbreak involves antibiotic-resistant Pseudomonas aeruginosa, primarily affecting users of EzriCare and Delsam Pharma eye drops. The FDA and CDC have warned against these products, leading to a recall by Global Pharma Healthcare. Efforts are underway to contain the outbreak, with healthcare facilities enhancing infection control measures. Individuals experiencing symptoms are advised to seek medical attention promptly. Public health campaigns emphasize the importance of hygiene and using safe products.