Product Liability

Published on: July 5, 2022

Recall of Medtronic’s HeartWare HVAD System Batteries

body-ge72aa36f3_640 Recently, Medtronic recalled HeartWare HVAD system batteries because of battery failure. The recall is categorized as Class I, the most significant recall, because the device may result in serious injuries or even death. Suppose you were injured due to a HeartWare HVAD system battery failure. In that case, you should consult the seasoned product liability lawyers of Moll Law Group about whether you have grounds to sue the manufacturer.

Call Moll Law Group About Your Medical Device Claim

The HeartWare Ventricular Assist Device (HVAD) System is utilized to keep the heart pumping blood to the remainder of the body. The system is implanted in patients’ bodies to bridge cardiac transplants used to help the heart when at risk of death from end-stage left ventricular heart failure. Doctors use these systems for heart tissue recovery or destination therapy (DT) in patients for whom heart transplants are not planned. The manufacturer, Medtronic, Inc., has recalled many batteries because they have welding defects. These defects allow the two cell battery packs to separate. This separation can result in a battery malfunctioning because power is not provided, and the battery cannot sustain a full charge or adequately recharge. The battery can fail suddenly.

A Power Disconnect alarm on the controller scene and in the Alarm Log tab is triggered when a malfunction happens. While these alarms may temporarily resolve, the battery may continue to fail. The result may be death or severe injury. The company has reported one death in connection with the recall, along with two complaints about united in the recalled lot. This year, Medtronic sent an Urgent Medical Device Correction letter to those affected, asking them to identify whether they have an affected battery immediately and to quarantine them accordingly. Doctors have been asked to notify patients with affected batteries and remove them from service; they have been given patient templates to inform patients about the harm. If you believe you may have been affected, you should discuss your situation with your doctor. The company is replacing impacted batteries with new ones and implementing actions to improve the batteries.

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Published on: June 28, 2022

FDA Forces Juul To Cease Sales

By Moll Law Group

eliquid-gf058e9070_640 On June 23, 2022, The U.S. Food and Drug Administration created an order against JUUL Labs Inc. to immediately remove their products from the market. These products are the JUUL itself and their entirety of different JUULpod types: Virginia tobacco and menthol flavored pods, both offered at nicotine concentrations of 5.0% and 3.0% respectively.

The company was added to Marketing Denial Orders (MDOs) with over 250 other similar electronic vapor products. This supports FDA belief that the positive aspect of aiding former smokers to quit does not outweigh the harm to young people, including but not limited to addiction, mental illness, and respiratory conditions.

FDA Commissioner Robert M. Califf, M.D. shared more on what prompted the movement.

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Published on: June 23, 2022

Supreme Court shuts down Bayer’s attempt to stop Roundup litigation

By Moll Law Group

On June 21, 2022 The United States Supreme Court denied an appeal to put an end to thousands of pending lawsuits tying Bayer’s weedkiller product to cancer diagnosis.

This development comes after a Supreme Court request from May of 2022 to hear from President Biden’s administration. Biden’s solicitor general produced a brief which urged the Court to the similar and recent rejection.

The decision supports a $25 million verdict from Northern California, awarding Edwin Hardeman damages from his continual Roundup use. While this case has been used in a practical sense of applying similar suits, Bayer has recently won four consecutive trials in various state courts.

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Published on: June 21, 2022

Asweets Recalls its Baby Activity Push Walker

By Moll Law Group

nepali-boy-gd20405235_640-e1655154307548 Parents may be alarmed to learn that Asweets has recalled its wooden baby activity push walker due to a strangulation hazard. The rubber rings on the rear wheels of a walker may separate from the wheels and detach, and this can result in a young child being at risk of strangulation. Asweets has received 10 reports of the rubber rings detaching from the wheels, though no injuries to babies have been reported. On June 2, 2022, the company recalled these walkers. If your baby is injured by an Asweets walker, or another walker that may be defective, you should give the experienced product liability lawyers of Moll Law Group a call. Cases with which we’ve been involved have resulted in damages in the billions.

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The remedy for the recalled Asweets baby walkers is a repair of the walker. The repair involves free replacement rear wheels. It’s important to take recalled walkers away from your children and stop using them until they are repaired. Around 13,300 units were affected by this recall. You can contact Asweets directly to get instructions on how to get replacement rear wheels. Retailers that sold the affected walker included Crate and Barrel, Nordstrom, Albee Baby, Bloomingdale’s, The Tot, and children’s boutiques.

However, in some instances, babies are injured by defective walkers, and a simple replacement really part doesn’t address the family’s needs. When you buy your baby a walker, you anticipate that it will be reasonably safe to use, and you don’t expect to incur medical bills because you allowed your baby to use it. Unfortunately, babies have been seriously injured while using various types of walkers their parents or caregivers assumed were safe. If your baby is injured by an Asweets walker, or any other kind of walker, you may not have enough saved to address the injuries and you may wish to consider bringing a product liability lawsuit for damages.

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Published on: June 14, 2022

Safety Hazards Cause Recall of Thousands of Units of Bed Rails

By Moll Law Group

healing-gbed9cb701_640-e1655154009557 Portable bed rails are installed on the sides of beds used for the elderly or those with medical conditions that increase the likelihood of falls from the bed. Unfortunately, bed rails can also present dangers. In April, the Consumer Product Safety Commission recalled thousands of units of bed rails over the last several months. Unfortunately, bed rails can present a safety hazard such that a consumer is entrapped and in danger of asphyxia and brain injuries or even death. The seasoned product liability lawyers of Moll Law Group may be able to help you if you or a loved one was injured as the result of using a bed rail.

Call Moll Law Group If You Were Injured or Lost A Loved One Due to a Defective Bed Rail

CPSC has issued warnings in connection with bed rails made between 1992 and 2021 by Mobility Transfer Systems Inc. It also issued warnings to stop using bed rails made by Metal Tubing USA Inc. in 2021-2022. The bed rails that were the subject of warnings were sold several places online including Amazon.com, Walmart.com, Alimed.com, VitalityMedical.com, MTS MedicalSupply.com, and eBay.

It has been reported that at least three people in different states died after entrapment in connection with the recalled models of the bed rails. These included a 78-year-old woman in an assisted living facility in, an 85-year-old man in a nursing home, and a 90-year-old disabled woman. The bed rails are made of white or chrome metal tubing, ad are labeled on the grip handle with “Mobility Transfer Systems.” The models include Freedom Grip, Freedom Grip Plus, Freedom Grip Travel, Reversible Slant Rail, Transfer Handle, Easy Adjustable, 30-inch Security Bed Rail, both single and double sided.

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Published on: May 31, 2022

Generac Electric Start Pressure Washer Recall Based on Malfunctions

By Moll Law Group

cleaning-gba057c9bd_640 Generac and DR Power brand electric start pressure washers with certain model numbers have been recalled. The washers have gasoline-powered engines, but electric start/stop buttons that are powered by a rechargeable battery. If you are a consumer, you should check whether your pressure washer is one of the models that has been recalled. Additionally, consumers injured by these washers or the families of loved ones who have died as the result of defective washers, may have a claim for damages and should call the experienced lawyers of Moll Law Group for a consultation.

Consult Moll Law Group About Your Pressure Washer Claim

Model numbers DPW3100DEN, DPW3101DEN, DPW3102DEN, G0071320, G0071321, G0071430 and G0071431 of the Generac and DR Power brand electric start pressure washer have been recalled. Their electronic start/stop buttons can malfunction, which means the means that the machine may self-start and thereby create a danger of carbon monoxide poisoning when the unit is located in a closed space.

Around 53,000 units of this washer were sold from February 2018 through February 2022 for $450 -$650. They were made in the United States and sold in major home improvement and hardware stores. Online retailers who sell them have included Home Depot, Ace Hardware, Lowe’s Stores, Amazon, Walmart, City Electric Supply, Costco, Do It Best, eBay, Essendant, Fastenal, Menard’s, Orgill, Power Equipment Direct, Ravitsky Bros., Tractor Supply, and True Value.

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Published on: May 24, 2022

Children’s Robes Were Recalled Because of Federal Flammability Standards Violations

By Moll Law Group

bathrobe-g1099931c3_640 Recently, Linum Home Textiles recalled those units of its children’s robes that failed to meet the federal flammability standards for children’s sleepwear because they present the risk of burn injuries to children. The company is offering a refund. If your child suffered burn injuries due to robes or other clothing that didn’t meet flammability standards, you should call the seasoned product liability lawyers of Moll Law Group. Billions have been recovered in lawsuits with which we’ve been involved.

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The manufacturer is recalling 100% combed Turkish cotton terry robes for kids. These are hooded robes with long sleeves that were sold in large, medium, and small sizes. Their colors are purple, gray, pink, navy, and white. Around 44,600 of the recalled robes have been sold. A refund is being offered for them. Washing instructions are set forth on a side-seam label sewn into the robe. If your child has one of the recalled robes, you should take it away and get in touch with Linum Home Textiles, which should send you a pre-paid mailer and instructions on how to return the robe for a refund.

Some of the robes were bought directly from Linum Home Textiles. However, they were also sold online from July 2017 – April 2022 at Wayfair.com, JCPenney.com, Bedbathandbeyond.com, Kohls.com, Zulily.com, Houzz.com, QVC.com, Overstock.com, Amazon.com, Groupon.com, Boscovs.com, Linumtowels.com and TorreyCommerce.com.

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Published on: May 17, 2022

AmazonBasics School Classroom Stack Chairs Have Been Recalled

By Moll Law Group

school-g843709daa_640 In April of this year, AmazonBasics school classroom stack chairs were recalled. According to the United States Consumer Product Safety Commission (CPSC), the weld on the chair’s frame may fail and present risks of falling. If your child was injured while using an AmazonBasics stack chair, you should call the experienced product liability lawyers of Moll Law Group. We are dedicated to consumers’ rights, and billions have been recovered in cases with which we’ve been involved.

Consult Moll Law Group About Falls from Defective Chairs

The AmazonBasics School Classroom stack chairs that present fall hazards are made of durable plastic with chrome-plated legs. Recommended for kids ages 3 -6 who weigh no more than 190 pounds, these chairs are stackable and sold in sets of six with red, purple, blue, yellow, lime green and pink. They measure 17 inches long and 15 inches wide and 26 inches high. If you have one of the recalled chairs, you may be entitled to a refund.

Around 22,400 units were sold online at Amazon.com between January 2019 – January 2022 for $128 -$190. There have been 55 consumer reports of the chairs breaking.

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Published on: May 12, 2022

Biden Administration Makes a Request of the Supreme Court in Roundup Weedkiller Case

By Moll Law Group

man-gba9125107_640 On May 10, 2022, President Joe Biden’s administration responded to the Supreme Court’s request that it provide its views on Roundup weedkiller litigation. Plaintiffs pursued claims against the manufacturer of Roundup weedkiller, Bayer, because evidence surfaced that Roundup may have caused their cancer. In the course of the litigation, Bayer had tried to evade liability by asking the Supreme Court to dismiss customer claims. When asked to weigh in, Biden’s solicitor general filed a brief asking the Court to reject Bayer’s request. In most cases, the Court defers to the solicitor general’s conclusions, so this is a crucial moment in the litigation. If you were diagnosed with non-Hodgkin’s lymphoma and exposed to Roundup, you should call the experienced product liability lawyers of Moll Law Group, which represents plaintiffs around the country. Billions have been recovered in cases with which we’ve been involved.

Talk to the Product Liability Lawyers of Moll Law Group About Your Claim

The brief from the Biden administration may have an impact on whether Bayer is willing to settle claims in the Roundup litigation. Court-watchers are closely scrutinizing whether the Supreme Court takes up Bayer’s request for review of a Northern California case because there are thousands of Roundup cases and many people who may be affected by the Court’s decision.

The Northern California case about which Bayer seeks review was brought by a Roundup user, Edwin Hardeman. He alleged that his cancer had been caused by Roundup and received $25 million in damages in a lower court decision. He had regularly used the weedkiller at his northern California home before getting diagnosed with a type of non-Hodgkin’s lymphoma. The Ninth Circuit had upheld this damages award in May. It was just one of many lawsuits alleging that the manufacturer should have warned consumers about the alleged cancer risk.

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Published on: April 29, 2022

Infant Formula Litigation Transferred to Multidistrict Litigation

By Moll Law Group

drinking-milk-gd45eea696_640 It is important to be aware that specific powdered infant formulas such as Similac and Enfamil have been linked to causing necrotizing enterocolitis in premature babies. Manufacturer Abbott Laboratories, Inc. made a motion before the United States Judicial Panel on Multidistrict Litigation to centralize the infant formula lawsuits pending against them in the District of Connecticut. In the cases to be transferred, the harmed plaintiffs contended that their infant formula, based on milk, causes necrotizing enterocolitis (NEC) when given to premature babies. If you believe your premature baby suffered from necrotizing enterocolitis and was injured or died because of infant formula, you may have a claim that can be heard as part of multidistrict litigation (MDL). Give the seasoned product liability lawyers of Moll Law Group a call. Billions have been recovered in cases with which we’ve been involved.

Discuss Your Infant Formula Case with Moll Law Group

The motion to transfer the lawsuits involving powdered infant formula to a district court in Illinois was supported by Mead Johnson Nutrition Company and Mead Johnson & Company, LLC. The plaintiffs agreed that it would be appropriate to centralize the 16 cases pending in 7 districts, along with 20 possibly-related lawsuits in 8 districts.

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