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Defective Products

Dehumidifier Recall: Several Brand Name Humidifiers are Recalled as a Fire Hazard

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The U.S. Consumer Product Safety Commission (CPSC) ordered Gree Electric Appliances to initiate a recall of 2.5 million dehumidifiers following a reported 450 fires related to the products overheating, smoking and catching fire.

Specific Models Being Recalled

The recall consists of units manufactured by the following companies: SuperClima, De’Longhi, SoleusAir, Fedders, Seabreeze, Fellini, Premiere, Danby, Frigidaire, Norpole, GE, Gree and Kenmore. The size of the manufacturer models includes: 70, 65, 50, 45, 40, 30, 25, and 20-pint dehumidifiers.

To find out if your unit is included in the recall, check the model numbers and date codes found on stickers on the front, back, or side of the unit. They come in gray, white, beige and black plastic housings. The units can measure from 19 to 24 inches in height, 13 to 15 inches in width with a 9 to 11 inch in depth. To determine if your unit is among those affected by the recall contact the manufacturer or the CPSC for details.

Dangers of Fire and Smoke

Many dehumidifiers are used in in workshops, garages, cellars and damp basements or other less inhabited areas of the home that are susceptible to moisture. The dehumidifier aids as a means of reducing the humidity in an affected area which in turn reduces the risk of mildew and mold formation that can trigger allergic reactions to those exposed. For this reason, if a unit overheats and catches fire it may not be immediately noticed which can lead to destructive fires. Additionally, the defect can be responsible for producing smoke in a fire which raises the risk for smoke inhalation related health problems and potentially death from oxygen deprivation. This situation becomes even worse if it happens at night when people are asleep and may take longer to react and get to safety.

Smoke inhalation can be a health danger as it causes irritation to nasal membranes, eyes, alveoli and brachii and other lung tissue. Smoke inhalation causes upper and lower respiratory irritation and infection and may exacerbate existing pulmonary conditions such as Chronic Obstructive Pulmonary Disease (COPD) and bronchitis. In people with seasonal allergies, this can adversely affect the natural recovery from infections brought on by pollen and other allergens that lead to colds, sinusitis or other respiratory conditions.

Damages Due to Defective Dehumidifiers

Over 2000 incidents have been reported on these products leading to over 400 injuries and more than $19 million in damages. The manufacture is offering refunds. If your unit is among those affected, you should initiate contact with them for a refund. This product is in its fourth recall since September of 2013. To eliminate your concerns of a fire, immediately unplug your dehumidifier and search for the manufacturer and the model of the unit.

These units were sold at several department stores, including Walmart, Sears, Sam’s Club, Mills Fleet Farm, Menard’s, Lowe’s, Kmart, Home Depot, HH Gregg and Aafes. Online these units were sold at Amazon and Ebay. All of these units were manufactured in China by Gree Appliances.

If you are concerned that your unit may be on the list of the makes and models being recalled, you can contact your manufacturer or the CPSC to verify if your unit is included. For additional information, you may contact Gree, Toll Free at 866-853-2808.

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Defective Products

Bayer Settles 90% of U.S. Essure Claims for 1.6 Billion

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About 90 percent of the more than 39,000 lawsuits filed against Bayer over Essure injuries have been resolved by a $1.6 billion settlement. Bayer said in a statement that the settlement resolves most filed and unfiled cases and that it continues to work with plaintiff’s lawyers to resolve the remaining cases.

FDA Actions and Essure Injury Complaints

The settlement comes after years of complains of adverse events involving the metal coils which are placed in the fallopian tubes. Some of these complaints say that the coils can perforate the tubes, tear the uterus, and that the coils can break causing little metal shards to migrate elsewhere in the body. Women have also complained of heavy bleeding, pain, and other side effects that the patients were forced to undergo hysterectomy.

In 2018, the U.S. Food and Drug Administration placed restrictions on the device and required patients to review the Patient- Doctor Discussion Checklist and sign prior to being implanted with the birth control device. Bayer made the decision to stop selling Essure in the United States not long after citing declining sales.

Post-Market Surveillance Reports

The required 522 study, a post-marketing surveillance plan, was also extended by the FDA from three to five years. The FDA published the first spreadsheet of Essure adverse events on August 11, 2020, which includes events that Bayer knew or learns of during the period of November 2016 to November 2020.

The first spreadsheet includes more than 1,400 events including pain, device fragments, pregnancy, and organ perforations, including 1376 reports of serious injury, 53 reports of death and 24 reports of malfunction.

Essure Lawsuit Settlement

Many of the plaintiffs alleged in court filings that Bayer knew or should have known about the risk of adverse events, including organ perforation, device breakage, and device migration. They also allege that Essure birth control was improperly design and can break and migrate after being implanted. They accused Bayer of misrepresenting the efficacy and safety of the contraceptive device and Women who suffered Essure injuries alleged in court filings that Bayer concealed the risks and dangers of the device from the FDA, the medical community and from the women who relied on the device.

Many of the terms of the settlement are confidential, and Bayer did not admit to any wrongdoing in the court filings.

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Covid-19

Risk for COVID-19 Goes Up for Vapers

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A new study shows the correlation between COVID-19 and young adults who are vaping. This includes teens as well. According to the study, the risk for developing the infection was five times higher if the person vaped regularly.

The study also indicated an increase of seven times the risk for young adults who vape and smoke tobacco cigarettes. The study was published in the Journal of Adolescent Health. Because of this information, the government has asked the US Food and Drug Administration (FDA) to remove all e-cigarettes from the market until after the pandemic has been dealt with.

E-cigarettes and Damage to the Lungs

Experts are concerned about the high numbers. They want young adults and teens to be aware that e-cigarettes and vaping devices aren’t safe. They come with serious harm that is real.

The evidence isn’t astounding, but it is important. It is well-known that e-cigarettes can harm the lungs as well as the immune system. In 2019, there were numerous cases of a mysterious lung illness associated with vaping. Many people got sick from the illness after vaping, and several people died.

There is another correlation between vaping and COVID-19. According to researchers, the SARS-CoV-2 virus that causes COVID-19 needs a pathway to get into the body’s cells. It is believed that e-cigarettes might make the pathway easier to access.

Another risk is that teens and young adults often share vaping devices. If one person is positive for COVID-19, the next person using that device could become infected as they inhale the virus right into their lungs. Exhaling from the vaping device could also cause people nearby to become infected.

The government is interceding in light of this news. The Subcommittee from the US House Committee on Oversight and Reform is calling on the FDA to get these products out of the hands of consumers. The subcommittee is the Economic and Consumer Policy.

This information goes along with a study from China that showed smokers in that country developed more serious symptoms and had to be hospitalized more often than other patients.

Young People Who Vape and Smoke are At Risk

An online survey was handed out in early May to teens and young adults under the age of 25. About half of the 4300 surveyed admitted to using e-cigarettes. The study showed that those who vaped had about three times the likelihood for being tested for COVID-19. Those who vaped and smoked had a five times higher rate of developing symptoms of the virus. These symptoms include coughing and fever as well as difficulty breathing and feeling fatigued.

Many young adults are already hooked on vaping and e-cigarettes. However, there are some programs that are tailored just for younger adults.

Some researchers also say that a direct correlation between e-cigarettes and COVID-19 hasn’t been made. While they believe that tobacco products do cause damage to the respiratory system and increase the infection rate, they cannot say for a fact that it causes an increased risk directly. However, all can agree that it appears that those young people who are using e-cigarettes are at a high risk for developing the coronavirus and possible complications.

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Defective Products

FDA Sets Limit for Acceptable Amount of Arsenic in Baby Cereal

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Cereal can contain arsenic from the grains it uses, but rice cereals are often higher in this toxic substance. The FDA has issued a limit for the amount of arsenic that can be found in rice cereal for infants. It is the first limit the agency has set up for arsenic in any food.

Arsenic in Baby Cereal

Rice is a grain with a high absorption rate for arsenic. It can end up with 10 times more of the metal than other grains. Because rice cereal is usually one of the first solid foods given to babies, it can have a significant impact on development.

Babies may eat multiple servings of rice cereal in a day, which can lead to exposure to inorganic arsenic, which is toxic. It can damage the neurodevelopmental system and harm their IQ.

Arsenic in rice cereal isn’t a new issue. Testing revealed that over 60 percent of rice cereals and other products have arsenic in them back in 2012. Since then, agencies have called for limits on the amount found in these products. Now, eight years later, the FDA has determined a limit of 100 parts per billion for arsenic in infant rice cereal. Other agencies have called for a lower limit.

While this limit is important news to manufacturers of baby cereal, it’s not enforceable. It is voluntary for manufacturers to follow these guidelines. The FDA conducted tests in 2018 on baby rice cereals, looking at the amount of arsenic present. About three-fourths of the products were at or below the new 100 ppb limit.

While critics believe this is an important first step to controlling the amount of arsenic that enters an infant’s system, they say more still needs to be done. Other products should be included, according to consumers advocates. Apple Juice is another product of concern. Experts believe it should be treated the same as drinking water with a limit of 10 ppb.

The Dangers of Arsenic

According to consumer advocates, limits should be given for all heavy metals, including lead and cadmium. The goal should be lower to reduce risk for children.

Arsenic is a natural element, which means it occurs in nature. It can get into the food supply through the soil as well as in the water and air. Contamination can happen with mining or fracking. Volcanoes that erupt can create an increase in arsenic at the surface of the earth.

Long-term exposure of arsenic has been linked to certain types of cancer and skin disorders. Even short-term exposure can lead to nausea and vomiting and other side effects. Young children have a higher risk for learning and development issues, which is why the FDA monitors products for infants and younger people at a higher rate than with other products.

It is important for parents to be aware of these risks and to determine which products are safest for their children. The effects from exposure to arsenic may not be seen right away, but they may be serious.

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