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Huish has recalled Oceanic brand SCUBA Diving Buoyancy Compensating Devices due to a potential drowning risk from faulty weight pocket handles. Affected models include Oceanic OceanPro, Excursion, and Hera, with about 7,445 units recalled in the U.S. and Canada. Users should stop using these devices and contact Huish for free replacement pockets. No injuries have been reported, but 73 handle failures have occurred. The recall was announced on June 15, 2023, covering products sold from April 2019 to May 2023. Legal recourse may be available for families affected by related accidents.

Zuru has recalled 7.5 million Baby Shark bath toys due to risks of impalement, laceration, and puncture injuries from their hard plastic top fins. The recall affects both full-sized and mini versions sold from 2019 to 2023. Consumers should stop using the toys and contact Zuru for a refund. Parker Waichman LLP offers legal assistance for injuries related to these toys, providing free consultations and handling cases on a contingency fee basis. They have a strong track record in product liability lawsuits.

Trek Bicycles is recalling nearly 97,000 units equipped with Promax hydraulic disc brakes due to a potential hazard where the brake hose may detach, posing a crash risk. The recall affects specific models with Promax Solve DSK-925 and Promax F1 DSK-927 brakes. No injuries have been reported despite 195 incidents of detachment. Owners should stop using the bikes and contact Trek dealers for free inspection and repair. Legal options are available for those affected by accidents due to this defect.

New York legislators have passed a bill to amend the 1847 wrongful death law, allowing claims for emotional damages and expanding eligible claimants. The bill, known as the Grieving Families Act, awaits Governor Kathy Hochul's decision. Hochul previously vetoed a similar bill in 2022, citing economic concerns and lack of a financial impact study. The 2023 version addresses some of her concerns but still lacks a financial analysis. Supporters argue the reform is overdue, while opponents worry about economic impacts. The bill's fate remains uncertain as it awaits Hochul's signature.

BearCare, Inc. has recalled the Walnut Wearable Smart Thermometer (model WT20, batch 20221115W002) due to risks of overheating and chemical leaks, which can cause severe injuries or death. The recall affects 979 units distributed in the U.S. from December 2022 to April 2023. Consumers should stop using the device, seek medical attention for any injuries, and return the product to BearCare. Legal assistance is available for those affected. For more information, contact BearCare at recall@walnutcares.com.

The FDA discovered significant sterilization failures at Global Pharma Healthcare's facility, linked to a fatal outbreak of bacterial infections in the US. The recall of EzriCare and Delsam Pharma's Artificial Tears followed reports of infections, vision loss, and fatalities. An FDA investigation revealed deficient manufacturing processes compromising product sterility. The outbreak involved a rare, drug-resistant bacteria, Pseudomonas aeruginosa, affecting multiple healthcare settings. The FDA emphasizes the importance of infection control and urges the public to stop using the recalled products.

On June 16, 2023, the FDA issued draft guidance to address potential contamination in tattoo ink, highlighting risks of infections from pathogens in unsanitary manufacturing conditions. Dermatologists warn of infections like rashes and abscesses from contaminated ink, often containing bacteria like nontuberculous mycobacteria. Despite the popularity of tattoos, with 30% of Americans having one, the guidance stresses the importance of understanding medical risks. Reputable manufacturers use gamma radiation to sterilize ink, but regulatory oversight is limited, leading to varied sterility and quality.

A civil lawsuit has been filed against Olaplex, a popular hair care brand, by Jessica Auriana and over twenty other women, claiming the products caused hair loss, bald patches, and other issues. Auriana noticed significant hair loss after using Olaplex products for two months. The lawsuit, filed in California, seeks over $75,000 in compensation for damages. Olaplex denies the allegations, asserting their products are safe and effective, and attributes hair issues to various external factors. The company is prepared to defend against these claims.

The FDA issued a warning letter to iRhythm Technologies regarding their Zio AT mobile cardiac telemetry device, highlighting several compliance issues. iRhythm failed to report two deaths and other medical device reporting breaches within the required 30-day period. The company also promoted the device for unauthorized uses, made unapproved modifications, and did not address customer complaints. The FDA's inspection revealed significant deficiencies in iRhythm's manufacturing and quality management systems. iRhythm's marketing claims misrepresented the device's capabilities, suggesting it was suitable for high-risk patients, which is not approved.

The U.S. Federal Trade Commission (FTC) has accused Amazon of deceptive practices by enrolling consumers into Amazon Prime without explicit consent and making it difficult to cancel subscriptions. The FTC claims Amazon used manipulative user-interface designs, known as 'dark patterns,' to mislead users. This lawsuit is part of a broader effort by the Biden administration to limit the power of big tech companies. Amazon denies the allegations, asserting that the Prime subscription process is transparent. The FTC seeks civil penalties and a permanent injunction to prevent future violations.

Research Products has recalled certain steam humidifiers due to a fire risk from 'D' shaped electrode connector wires that may overheat. Consumers should stop using these units and contact the company for a free repair kit. The recall affects about 36,200 units in the U.S. and 3,800 in Canada, sold from 2010 to 2015. There have been 103 overheating reports, including 10 fires. Affected brands include AprilAire and Carrier. For legal assistance, Parker Waichman LLP offers consultations for potential product liability claims.

The FDA has initiated an independent study of the U.S. baby formula industry due to safety and regulatory concerns. Conducted by the National Academies of Sciences, Engineering, and Medicine, the study will address supply challenges, market characteristics, and regulatory disparities between the U.S. and the EU. This effort is part of the Food and Drug Omnibus Reform Act of 2022. The study follows a difficult year marked by recalls and shortages, with findings contributing to a long-term national strategy to improve market resiliency.

Draeger Medical has recalled 570,459 infant breathing therapy devices due to a manufacturing defect in the Seattle-Positive Airway Pressure Plus system and related products. The defect involves potential loosening of glued hose connections, risking oxygen supply and posing severe health threats. The FDA classified this as a Class 1 recall, the highest risk level. No injuries have been reported. Affected customers should stop using these devices and contact Draeger for replacements. The recall follows similar issues with Philips CPAP machines, which have led to numerous health complaints and legal actions.

The U.S. Consumer Product Safety Commission (CPSC) has issued a warning and plans to recall fire extinguisher balls sold on Amazon due to safety concerns. Brands like LVYXON, TATTCHINE, and others are implicated. These products may fail to extinguish fires and lack essential safety features. The CPSC advises against using these items and recommends disposing of them at a fire station or hazardous waste facility. Fire extinguisher balls are spherical devices that activate when exposed to fire, releasing chemicals to extinguish flames. They are typically red, 4-7 inches in diameter, and come with a wall-mountable stand.

TJX has recalled approximately 10,850 Haining Degao Benches due to a fall hazard, as the legs can break or detach, posing a risk of injury. The recall affects benches sold at Marshalls and T.J. Maxx from December 2021 to March 2023. Consumers should stop using the benches and can return them for a full refund. TJX has received 21 incident reports, with 17 resulting in injuries. For more information, consumers can contact TJX or visit their recall website.

New York has enacted the Warehouse Worker Protection Act, becoming the second U.S. state to regulate warehouse work quotas, following California. The law, signed by Governor Kathy Hochul, aims to improve conditions for Amazon workers by banning quotas that hinder breaks and mandating written quota notices and productivity data. This legislation responds to reports of injuries linked to Amazon's productivity demands. Unlike California's law, New York's version lacks provisions for safety interference and worker lawsuits due to time constraints. Amazon disputes the need for the law, citing misunderstandings of its practices.

On June 13, the FDA announced a recall by Willamette Valley Fruit Co. of various frozen fruit products due to potential hepatitis A contamination. The recall affects Walmart's Great Value brand, including Sliced Strawberries, Mixed Fruit, and Antioxidant Blend, distributed in 32 states. Other retailers like Costco and HEB are also recalling specific products. No illnesses have been reported, but consumers are advised to discard or return the products. Symptoms of hepatitis A include fatigue and jaundice. Customers should consult healthcare providers if they suspect exposure.

The U.S. Consumer Product Safety Commission (CPSC) has issued a warning about Girasol Rainbow Love Woven Wrap sling carriers, advising consumers to stop using them due to a fall hazard. These carriers do not meet federal safety standards, lacking structural integrity and proper warning instructions. Despite the risk, the importer, Baby Earthling LLC, has not agreed to a recall. Consumers are urged to dispose of the carriers and report any incidents to the CPSC. The carriers were sold online until November 2022, priced between $120 and $165.

The Consumer Product Safety Commission (CPSC) and The Boppy Company have linked two additional infant deaths to recalled newborn loungers, urging consumers to stop using them. These loungers, recalled in September 2021 due to suffocation risks, are still being sold online illegally. Despite multiple requests to remove these products, they remain available on platforms like Facebook. The CPSC emphasizes safe sleep practices, advising that infants should sleep on firm, flat surfaces without additional items. Consumers are encouraged to participate in the recall and contact The Boppy Company for more information.

Allied Air Enterprises, in collaboration with the U.S. Consumer Product Safety Commission, has recalled approximately 9,255 Armstrong Air and Air Ease gas furnaces due to a carbon monoxide poisoning hazard. The recall affects units sold between September 2022 and March 2023, with model numbers A96UH1E045B12S, A96UH1E070B12S, and A96UH1E110C20S. Consumers are advised to contact Allied Air for a free repair to replace the faulty component. No injuries have been reported, but users should ensure carbon monoxide alarms are installed in their homes.

Chrysler is recalling around 330,000 Jeep Grand Cherokees due to improperly installed rear coil springs, which could detach and increase collision risks. The recall affects 2022-2023 Grand Cherokees and 2021-2023 Grand Cherokee L models. Chrysler urges owners to visit dealerships for free inspections and repairs. No injuries have been reported, but Chrysler received 17 warranty claims and two customer assistance records. Affected owners will receive recall details by July 28, and refunds are available for prior repairs with receipts. For inquiries, contact Chrysler or the NHTSA.

Empower Brands has recalled 469,000 PowerXL Self-Cleaning Juicers due to reports of injuries, including severe lacerations and ingestion of small fragments. The U.S. Consumer Product Safety Commission (CPSC) reported 261 incidents of the juicers breaking apart, resulting in 47 injuries. Consumers are advised to stop using the juicers and contact Empower Brands for a refund. The recall affects models SHL90-SC and SHL96, sold from September 2020 to August 2022 at major retailers and online. Refunds will be issued via prepaid Visa cards.

TopGlore has recalled Narskido Infant Bath Seats due to a drowning risk, as they do not meet federal safety standards for stability and leg slot dimensions. Sold exclusively on Amazon.com from May to September 2022, these bath seats can tip over, posing a danger to infants. Customers should stop using the product and contact TopGlore via Amazon for a full refund. The recall highlights the importance of product safety and the potential for legal action if harm occurs.

Philips' Respironics division is facing another Class I FDA recall for its Trilogy Evo ventilators due to potential device malfunctions linked to environmental contamination. This is the second recall in a few months, following previous issues with sound-dampening foam and a sensor problem. The recall affects around 120,000 devices globally. Philips has been proactive in addressing these issues, having manufactured over 98% of replacement devices and repair kits for previous recalls. The FDA is investigating the cause of the current problem.