We are happy to announce that we're celebrating 30 years! →

REQUEST FREE CONSULTATION
Published on:

By

Over 360,000 toddlers suffered injuries as a result of falling or tipping over during the years between 1990 and 2010. A Poland-based manufacturer called Lenny Lamb has recently come under fire for problems and risks associated with its Lenny Lamb brand child carriers. The company recently issued a recall for its buckle onbu infant carrier, even though it has not received any reports of specific injuries. The U.S. Consumer Product Safety Commission has not received any reports or information regarding injuries either.

According to media reports, nearly 1,000 of the onbu carriers were missing a key component. The carriers feature a strap used to secure the device, in which the infant is placed, to the wearer’s body. The affected products are missing internal stitching that ensures the child stays inside the sling device. The device is intended to be worn with the infant carried on the wearer’s back. This means that if the device fails, and the infant falls, the wearer will have a difficult time reacting quickly enough to save the child from harm.

The carrier also features a hood, interior adjustable panel, and shoulder pads. It retails for roughly $90. Affected units were sold online at Bibetts, Lenny Lamb, 5 Minute Recess, Cozy Cuties, and a variety of other outlets between May 2016 and June 2016. To learn more about which units may be affected by the product defect, visit the Consumer Product Safety Commission website.

Continue reading →

Published on:

By

In the recent case of Hosford v. BRK Brands, Inc., the Supreme Court of the State of Alabama considered whether a smoke detector manufacturer could be held liable for the death of the plaintiffs’ daughter, resulting from a fire in the family’s mobile home. The defendant in the lawsuit manufactured two smoke alarms that had been installed in the family’s mobile home prior to when the fire took place. In their complaint, the plaintiffs alleged that the manufacturer designed the smoke alarms in a defective manner and failed to provide sufficient warnings about the dangers associated with the fire alarms.

During the litigation, the plaintiffs conceded that one of the smoke detectors made an alerting sound at the time the fire began. However, they contended that the alarm did not sound soon enough to ensure that the occupants could exit the mobile home safely, which would have required rescuing their daughter before exiting.

The plaintiffs’ complaint included numerous causes of action against the defendant, including a breach of warranty claim, a failure to warn claim, and a negligence claim. They also asserted a product liability claim, which imposes a strict liability standard on the defendant. At the close of trial, the trial court judge concluded that the plaintiffs had only provided enough evidence to support their product liability claim. The jury deliberated and returned a verdict in the defendants’ favor. The plaintiffs appealed.

Continue reading →

Published on:

By

In a recent case in front of a state appellate court, a woman filed a medical malpractice lawsuit after she was treated for a condition known as thoracic outlet syndrome. The illness caused her extreme pain around her shoulder and in her arm and also caused her numbness, swelling, and weakness. As a result, she was treated by a doctor who performed a surgery to try to ease the pain by removing one of her ribs. However, the woman suffered severe symptoms after the surgery, including pain whenever she moved her arm and difficulty swallowing food. The woman then sued the doctor for malpractice.

The defendant presented an expert who said that the doctor performed the surgery correctly and provided proper post-operative care. The expert also said that the woman’s symptoms after the surgery were a result of her original illness. To rebut this, the woman presented her own expert, who was a doctor in Mexico. The doctor had examined her about one year before she sought treatment from the defendant. Her expert stated that the defendant had destabilized the woman’s right sternoclavicular joint during the surgery or had disrupted the ligaments that hold it in place.

The defendant objected to the plaintiff’s expert witness, arguing that he was not familiar with the “standard of care” in the United States. The trial court agreed and dismissed the case. However, a court of appeals found that her expert witness, who was licensed to practice medicine in Mexico, was qualified to give an opinion in this case. Importantly, the defendant doctor did not suggest that the standard of care in Mexico was different from the standard of care in the United States. In addition, the Mexican doctor had performed over 500 orthopedic surgeries and around 10 to 12 thoracic outlet syndrome surgeries. He also personally examined the woman before and after her surgery. Thus, the court found that he was qualified to give his opinion, and the jurors were free to give it as much weight as they determined was appropriate.

Continue reading →

Published on:

By

In the first pelvic mesh trial to go forward against Boston Scientific, the plaintiff obtained a victory from a Massachusetts court, which overturned a prior verdict rendered in 2014 that had dismissed the case. The plaintiff will now be able to proceed with a new trial. Boston Scientific’s pelvic mesh product has been the subject of thousands of lawsuits, resulting in the compilation of a Multi-District Litigation proceeding in West Virginia.

The plaintiff in the case, Diane Albright, contended that the company’s Pinnacle mesh product was designed in a defective manner and resulted in her experiencing serious injuries. The woman received the device to treat her pelvic organ prolapse condition. In July 2014, the jury hearing her case concluded that Boston Scientific designed the device properly and that it provided sufficient warnings about the risks associated with the product. The plaintiff appealed this verdict, stating that the lower court judge erred when it precluded the jury from hearing evidence regarding a material safety data sheet for the polypropylene that the company included in the mesh. The plaintiff argued that this MSDS document showed that the chemical was not appropriate for implantation in the human body.

The plaintiff also contended on appeal that the judge committed reversible error in preventing two letters from the FDA that were sent to Boston Scientific from being included in the evidence. The letters included directions from the federal agency ordering Boston Scientific to perform post-market surveillance studies for its mesh product. The letter also showed that the FDA agreed to suspend this order to perform studies after Boston Scientific said that it was no longer intending to sell the mesh product.

Continue reading →

Published on:

By

In a recent case decided by a state appellate court, a husband and wife were injured in a car accident with another motorist. After the accident, they filed suit against the motorist for their physical injuries, mental suffering, lost wages, and lost employment. However, the motorist failed to defend or respond to the lawsuit. As a result, after four months had passed, the couple filed an application for an entry of default against the motorist, and the clerk of the court entered a default judgment against him. Seven months after the complaint was filed, the motorist responded by filing a motion to set aside the default judgment. The court denied his motion to set aside the entry of default and entered a default judgment in favor of the couple for over $3 million.

The motorist appealed. He argued that the court abused its discretion by refusing to set aside the default judgment. That state’s supreme court found that since default judgments are considered under a liberal standard, the court did abuse its discretion by refusing to set aside the entry of default. It noted that the motorist had seemingly valid defenses to the claim. In addition, the couple would suffer limited prejudice by reopening the case because they filed the claim three years after the actual accident and were still litigating the case with two insurance companies. For these reasons, the default judgment was set aside, and the case was reopened.

Default Judgments and Illinois Rules

A default judgment is a ruling that results from one party’s failure to comply with the requirements of the court. A default judgment is binding on a party even if the person has never appeared in the case. That means that even if a defendant never appeared in court in a case against them, the other party can collect compensation. However, even if a default judgment has been entered against a party, they can file a motion to set aside the judgment and reopen the case.

Continue reading →

Published on:

By

In a tragic case of medical malpractice recently decided by one state appellate court, a woman underwent a liposuction procedure at a medical spa and tragically died just a few days later from septic shock. The woman’s husband filed a medical malpractice claim against the company, alleging that the bacteria causing the shock came from the medical spa during his wife’s procedure. He claimed that certain equipment had not been properly disinfected and sterilized.

The case went to trial once, but it resulted in a mistrial based on the improper questioning of a witness in front of the jury. The case was retried, and the jury found in favor of the woman’s husband. The jury awarded him over $3 million in damages. The spa appealed the decision. It argued that there was not sufficient evidence for the jury to find in favor of the husband.

The court explained that it would not set aside the jury’s verdict as long as it was supported by substantial and competent evidence. It also would not second guess determinations of credibility and the weight of the evidence made by the jury. In this case, there was a medical expert who explained how the spa’s procedures for sterilizing and disinfecting the reusable medical equipment used in the procedure breached the standard of care for cosmetic surgeons. There also was evidence that the spa’s breach caused the woman’s death because septic shock occurs after an infection causes the body to go into shock, and she had bacteria present near where she was injected. Even though there was some evidence presented by the defense suggesting that the bacteria could have come from her post-procedure care, the jury’s decision was still reasonable and would not be second guessed. Accordingly, there was substantial evidence supporting the jury’s verdict, and the decision was affirmed.

Continue reading →

Published on:

By

Many people are quick to blame parents for children’s injuries. Yet often, the parents are not to blame. Defective products such as toys, cribs, and baby carriers can cause children serious injuries.

If a defective product is to blame, a parent can sue the manufacturer or anyone else in the chain of distribution, seeking compensation for their child’s injuries. If a product is defective, it generally is defective by its design or has a defect in how it was made when it was manufactured. For example, a defective design might exist when a product has an unreasonably dangerous design, such as a stroller that too easily tips over. A manufacturing design might exist when a piece was left out when it was built, thereby creating a danger. A product could also be defective because the safety warnings are inadequate to warn the consumer of a potential danger associated with the product.

New Study Shows Injury Risk Posed by Strollers and Baby Carriers

A new study shows that over 17,000 children are treated in emergency rooms every year for stroller and baby carrier-related injuries. According to one news source, the study, conducted by the Center for Injury Research and Policy at the Nationwide Children’s Hospital, looked at emergency room visits from 1990 to 2010. It found that over these years, almost 361,000 children had been treated for such injuries. This equates to about two children an hour, or around 50 children per day.

Continue reading →

Published on:

By

A new lawsuit brought by a group of Oregon residents claims that Precision Castparts has released heavy metals and toxic chemicals into public areas. The class action complaint claims that the residents have been exposed to “hot spots” of these carcinogenic materials. The lead plaintiff in the lawsuit alleges that the company, which makes aircraft parts and engine parts, has emitted substances like arsenic and nickel, thereby contaminating businesses, homes, and public areas. If an individual is exposed to dangerous levels of arsenic and nickel, a number of devastating health conditions may result, including lung damage, nerve damage, and birth defects.

The complaint states that roughly 5,000 homes within the area have been exposed to toxic chemicals and that they will continue to suffer this exposure even if the company ceases its allegedly tortious activity. The named plaintiffs consist of four individuals who each live within one mile of the defendant’s business location. They allege that they have been deprived of the use and enjoyment of the area surrounding their homes as a result of the airborne contamination and that they have incurred damages as a result of having to purchase air filtration systems.

In a 2013 study performed by the University of Massachusetts, the company was deemed the worst industrial air polluter in the United States. Both the Oregon Department of Environmental Quality and the U.S. Forest Service have issued studies that name the defendant as one of the biggest polluters in Portland, stating that the company was responsible for much of the contamination in the citywide area. To reach this conclusion, the agencies performed tests on samples of moss from trees within the area. Since moss absorbs ambient pollutants from the surrounding air, it is a good indicator of the amount of toxic chemicals in the air.

Continue reading →

Published on:

By

In a recent case out of California, a man was injured in an accident with another car, driven by a paramedic supervisor. The paramedic was driving his employer’s truck on the way to the location of an injured victim when the accident occurred. The injured driver subsequently filed a negligence lawsuit against the paramedic. The state’s laws required that lawsuits against health care providers for “professional negligence” be filed within one year of the injury date. In this case, the man’s case was filed past the one-year filing date. As a result, the court found that the claim was time-barred.

However, a case from that state’s supreme court found that the time period applied only to negligence actions that resulted from services provided by virtue of being health care professionals—or in rendering medical care to patients. Thus, in this case, while the paramedic was a medical professional, the accident did not result from negligent medical care. The paramedic was required to drive the car with reasonable care because he was driving a car, not because he was providing health care to a patient because he was a paramedic. Thus, the decision was reversed, and the case was able to proceed.

Medical Malpractice Statutes of Limitations in Illinois

Every individual who files a claim has to consider the relevant statute of limitations. The statute of limitations refers to the time during which a claim must be filed. The time varies for different claims and depending on where the claims are filed.

Continue reading →

Published on:

By

The number of individuals who have been affected by the recent outbreak of Hepatitis A in Hawaii continues. The outbreak has been linked to a seafood importer and a sushi chain. A class action lawsuit has been filed against both entities, alleging various claims against them. According to the Hawaiian state health departments, the number of individuals who have contracted Hepatitis A as a result of the outbreak has climbed to 228. Based on this and other information regarding the outbreak, the estimated number of individuals who could end up contracting Hepatitis A or who have been exposed to Hepatitis A could reach 10,000.

The restaurant chain involved in the incident is called Genki Sushi, while the distributors involved include Koha Foods and Sea Port Products Corp. According to the Food and Drug Administration, scallops provided by the distributor and served by the restaurant were contaminated with Hepatitis A. The federal food safety agency has advised anyone who has eaten at Genki Sushi or who may have come into contact with an employee or someone related to the restaurant to seek medical care as soon as possible.

Continue reading →

Contact Information
180 N Stetson Ave 35th Floor
Chicago, IL 60601
T 312.462.1700F 312.756.0045E info@molllawgroup.com
We represent people nationwide including, but not limited to, those in the following localities: Atlanta, Baltimore, Boston, Chicago, Dallas–Fort Worth, Denver, Detroit, Houston, Los Angeles, Miami, New York City, Philadelphia, Phoenix, San Bernardino-Riverside, San Diego, San Francisco, Seattle, St. Louis, Tampa–St. Petersburg, and Washington, D.C.

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Please do not include any confidential or sensitive information in a contact form, text message, or voicemail. The contact form sends information by non-encrypted email, which is not secure. Submitting a contact form, sending a text message, making a phone call, or leaving a voicemail does not create an attorney-client relationship.

Copyright © 2025, Moll Law Group
JUSTIA Law Firm Blog Design