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A state court of appeals considered two cases in which underage people were consuming alcohol on an adult’s house and then drove, getting into an accident. The adults knew that the underage people were drinking alcohol but allowed the minors to do so. In one case, one of the underage drinkers caused the death of another person after driving drunk, and in the other case, the underage drinker caused another individual serious injuries. The plaintiffs claimed that the adults were negligent in allowing the minors to drink on their watch. The state’s supreme court held that adults who allow underage drinking can be held liable to those who are injured as a result, including the underage drinkers. In addition, the court held that in these two cases, the adults owed a duty to these victims.

A 17-year-old drank during a party at an adult’s house, and when he left early in the morning, still intoxicated, he was killed when riding in another intoxicated partygoer’s car. In that case, a woman’s underage son had friends over. His mother was home and knew that underage people were drinking, but she did not tell them to limit or stop drinking. She also did not attempt to prevent any guests from driving.

In the other case, an 18-year-old had been drinking with a 26-year-old and another friend at the 26-year-old’s house. The man knew that the 18-year-old was only 18, that he had too much to drink, and that he would have to drive home. The 26-year-old offered him a place to sleep but told him he could leave if he was “sure that he was going to be able to drive.” The 18-year-old left early in the morning, and while driving, he hit a woman walking her dog on a sidewalk, causing her life-threatening injuries.

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When we patronize restaurants, we expect that the people in charge have taken appropriate steps to ensure that the food we consume will be safe and free of adulterants. What fewer patrons realize, however, is that these safety measures extend to ensuring that the employees and servers who prepare and deliver our food are free of diseases and infections that could easily contaminate us and our families. Recent reports have indicated that there are at least 135 confirmed cases of Hepatitis A outbreaks in Hawaii, according to the Hawaii State Department of Health. This represents over 40 additional cases since the department issued an update during the last week of July.

According to this recent update, one of the affected victims in the rampant and ongoing outbreak of the dangerous Hepatitis A virus includes an employee who works at a Chili’s restaurant location in Oahu. Another employee includes a Hawaiian Airlines flight attendant. Both of these employees have had substantial exposure to the general public. Also, considering that Hawaii is a popular tourist destination, it is highly likely that someone who has come into contact with these two affected individuals or another carrier of the virus has since returned home and come into contact with countless other individuals. According to a Hawaii State Epidemiologist, neither the employee at Chili’s nor the flight attendant have been linked to any additional outbreaks, and neither outlet is being deemed a source of the outbreak.

Another restaurant, however, was not so lucky. Employees at Baskin-Robbins, a Taco Bell location, Cosco Bakery, and a sushi restaurant were also identified as carrying Hepatitis A. Nearly 25 employees at the sushi restaurant, Sushi Shiono, tested positive as carriers of Hepatitis A.

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In a recent case decided by a state appellate court, a 10-year-old boy was killed while riding as a passenger on a speedboat. While driving on a lake, the driver of the speedboat drove the speedboat between two warning buoys and hit a submerged pipe. The mother had taken her four children fishing on a lake with her boyfriend when the accident occurred. The boy’s mother settled claims against the boat’s driver and others, and then she sued the state’s Department of Natural Resources. The mother argued that the state was liable because it marked the pipe with buoys that were too far apart, the pipe’s placement violated state laws, the pipe was concealed, and the pipe posed a danger to individuals.

The state’s supreme court dismissed the case, finding that the public duty doctrine barred the mother’s claim. The court explained that the public duty doctrine means that if a duty is owed to the public in general, there can be no liability to an individual who is a member of the public. However, there may be a duty to an individual if a special relationship existed. In effect, the public duty rule acts to protect municipalities from liability arising from failing to adequately enforce laws and regulations.

Here, the court found that there was no special relationship between those on the lake that day and the Department of Natural Resources. Members of the public can use the lake at no cost and come and go as they please. There was a duty owed to the general public but not to individuals, and there was no special relationship between the state and recreational boaters. Thus, the claim was barred by the public duty doctrine.

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The U.S. Food and Drug Administration has recently issued a safety alert for Wen hair conditioner products. According to the federal agency, these products may result in severe breakage, balding, rashes, itching, and hair loss. The products are the subject of ongoing litigation that was commenced in 2014 through a class action lawsuit. The low-lather conditioners, which were developed by celebrity stylist Chaz Dean, have been the subject of over 127 FDA complaints from consumers.

According to the safety alert, this issue constitutes the most reported adverse event associated with a hair product. In addition to the 127 complaints sent to the FDA, roughly 21,000 complaints were delivered to Chaz Dean, Inc., by consumers who used the product and experienced negative consequences.

The FDA safety alert states that the reason behind the adverse side effects is unknown and that the company that makes Wen cleansing conditioner products has been asked to provide data that could help the consumer safety agency determine the issue. There are a variety of ingredients in the products, many of which are harmless. Chamomile, aloe vera, soy protein, and almond oil are examples. A few ingredients are not as benign, like methylisothiazolinone and methlchloroisothiazolinone. Both of these preservatives have been associated with eye, skin, and lung irritations. The Environmental Working Group prepared a report about the side effects and dangers associated with these preservatives.

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A woman filed a negligence case against a doctor after the doctor left a surgical sponge in her abdomen while she was undergoing gastric bypass surgery. The woman underwent a gastric bypass surgery in 2003, and she had several follow-up appointments in the subsequent years. The woman said that she began having uncomfortable sensations and pain in her stomach about one year after the surgery. The woman described these symptoms to her doctor at several follow-up appointments.

In 2009, she had a CT scan done for an unrelated condition, which revealed that she had a surgical sponge in her abdomen. She had it removed immediately. Less than a year later, the woman brought a medical malpractice claim against the doctor, seeking compensation for her medical expenses as well as for the pain and suffering she endured.

The defendants argued that the woman’s claim was barred because the statute of limitations had passed. The woman’s attorney argued that the claim was not barred, due to the “continuing course of treatment doctrine.” Under the state’s continuing course of treatment doctrine, a plaintiff generally needs to show that 1) there was a medical condition that required ongoing treatment or monitoring; 2) the defendant provided ongoing treatment or monitoring after the negligent treatment; and 3) the plaintiff brought the claim within the statute of limitations after the treatment ended.

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The Food Safety Inspection Service, which is the administrative arm of the USDA responsible for regulating food safety in the majority of food products containing meat, has issued a recall covering 8,800 pounds of ground beef from PT Farm, a New Hampshire-based operation. The ground beef is believed to be contaminated with the dangerous and potentially deadly pathogen E. coli. The recall covers products produced between June 6 and June 16, 2016. It was at this time that the first case of E. coli linked to the beef products was identified. Just last week, another individual was confirmed to be ill as a result of consuming E. coli-infected beef products.

E. coli symptoms can manifest in a variety of situations. For many people, fevers are common, along with gastrointestinal or stomach issues. Although affected individuals typically recover within five to seven days, there are some instances in which the individual must be admitted to the hospital. This is especially true for individuals with compromised immune systems, pregnant women, children, and the elderly. If you believe that you have consumed a food product that is contaminated with E. coli, it is critical that you contact a medical professional immediately to receive a proper diagnosis and medical attention.

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In a recent case, a man brought a claim against a church after he was hit by a car while he was crossing a road to go to the church. The man had just parked his car in an overflow parking lot, which was owned and staffed by a local church. He was going to attend an event at the church, and to get to the church he had to cross a busy five-lane road. The man and his wife sued the church, alleging that the church negligently located its overflow parking lot in an area that required churchgoers to cross a busy road and failed to provide churchgoers with assistance in crossing the road.

The church argued that it did not owe a duty to the man because it did not own or control the road he was crossing when he was injured. However, the appellate court found that the location of the church’s overflow parking lot exposed churchgoers to an unreasonable risk of injury. Specifically, it required them to cross a busy road where there was no marked crosswalk or traffic signal in order to cross the road and get to the church.

The court explained that those who own, possess, or control property have a duty to exercise ordinary care in managing the property so that others are not exposed to an unreasonable risk of harm. Even though the church did not control the street where the man was hit, it did control the location of the overflow parking lot, which could have contributed to his injury.

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The U.S. Food and Drug Administration recently issued a new warning increasing the cautions associated with fluoroquinolone-based medications, concluding that this class of antibiotics may be too strong to address bronchitis, sinus infections, and urinary tract infections. The FDA has received a number of complaints regarding the drugs and has concluded that dangerous side effects include disabling and potentially irreversible tendon, muscle, joint, nerve, and central nervous system pain. The warning label for these drug products has been updated to reflect these new risks.

The agency also stated in its warning that fluoroquinolones should only be prescribed to patients who have no other medical recourse for acute bacterial exacerbation of chronic bronchitis, uncomplicated urinary tract infections, or acute bacterial sinusitis. More specifically, health care professionals should immediately stop prescribing these medications for patients who have any of these conditions and support any serious adverse reactions as soon as possible. The current Boxed Warning for fluoroquinolone medicines applies to a number of conditions like tendon rupture, myasthenia gravis, and tendinitis, as well as peripheral neuropathy and a variety of other conditions.

Patients who have been injured as a result of taking dangerous pharmaceuticals can file a product liability or negligence claim against the drug manufacturer. The FDA requires drug manufacturers to comply with extensive regulations regarding the development, testing, approval, and marketing of new drugs. In many instances, companies that manufacture and sell dangerous pharmaceuticals have failed to comply with some of the testing requirements or even hidden information from the FDA about adverse side effects associated with the drugs when seeking approval.

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A 23-month-old boy tragically drowned in a pond after he climbed out of his crib and walked outside in the middle of the night. After the accident, the boy’s parents filed a product liability case against the company that manufactured the doorknob cover they had installed on their front door. The doorknob cover was a safety measure to prevent children from opening doors. The boy’s parents used the doorknob cover on the front door of their home to stop him from opening the door. However, the company argued that the doorknob cover was not defective or unreasonably dangerous if it were used properly.

At trial, evidence showed that after the boy began climbing out of his crib, to help ensure their son’s safety, the couple began using a chain lock on the front door in addition to the doorknob cover. On the night of the accident, the boy’s mother locked the tab lock on the doorknob but forgot to latch the chain lock. The boy was discovered the next morning, and the doorknob cover was on the floor in two pieces. Investigation notes with social services stated that the parents knew the boy was able to defeat the doorknob cover, which was why they installed the chain lock. However, the father denied making that statement.

The parents argued that evidence of their knowledge of the boy’s ability to defeat the doorknob cover should be excluded because it was irrelevant, and at most it was only a contributing cause but not the sole cause of the accident. They also argued that it was overly prejudicial. Despite their objections, the evidence was allowed at trial.

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In a recent case in front of a state appellate court, a woman died while in the care of a nursing home, and the woman’s daughter filed a wrongful death claim against the nursing home, alleging medical malpractice. In response, the nursing home filed a motion for summary judgment to have the case dismissed because the woman failed to designate an expert witness.

The woman then designated two expert witnesses. Subsequently, the court granted summary judgment because although the woman designated the experts, she failed to produce sworn expert testimony. The woman then filed sworn expert testimony by filing affidavits from the expert witnesses and requested a reconsideration of the judgment. The court denied the reconsideration motion. Under that state’s rules, sworn expert testimony is required in medical malpractice cases, and it is necessary to survive summary judgment.

The woman appealed and argued that the dismissal of the case was too harsh a sanction for a “discovery violation.” However, the court stated that the court did not impose sanctions because of her failure to follow discovery rules. Instead, the court dismissed the case because of a motion for summary judgment filed by the defendant, and she had failed to provide sufficient evidence to survive a motion for summary judgment. Accordingly, the state’s supreme court agreed with the decision and affirmed the dismissal.

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