The Consumer Product Safety Commission (CPSC) has announced Fitbit’s March 2, 2022 recall of its Iconic smart watches due to the risk of burn injuries. The company found that the lithium-ion battery in its smartwatch may overheat. Around 1 million affected Fitbits have been sold around the country. The remedy if…
Illinois Injury and Mass Tort Lawyer Blog
CPSC Complaint Against Leachco for the Podsters
Leachco, Inc. manufacturers infant loungers called the “Podsters.” After reports of two infant deaths in connection with these loungers, the company refused to undertake a voluntary recall. The United States Consumer Product Safety Commission (CPSC) filed an administrative complaint about the loungers against Leachco. The complaints concern Leachco’s Podster, Podster…
Hot Air Brushes Recalled Due to Danger of Electrocution or Shock
BrushX hot air brushes were recalled on February 17, 2022 due to the risks of electrocution or shock. If you were left with injuries due to electrocution or shock from a BrushX hot air brush, you should consult the experienced Chicago-based product liability lawyers of the Moll Law Group about…
Second Infant Died After Consuming Recalled Abbot Baby Formula
Recently, Abbot Nutrition expanded its recall of baby formula after a second baby died from infection after consuming the formula Abbot Nutrition’s Similac PM 60/40 with a lot code 27032K800. Four reports of Cronobacter sakazakii infection have been reported in connection with products from the plant. If your baby was…
Another Lawsuit Filed in Elmiron Multidistrict Litigation
Elmiron is a drug for bladder pain manufactured by Johnson & Johnson, its subsidiary Janssen Pharmaceuticals, and other parties for eye damages. If you suffered injuries due to Elmiron, you may have a claim that should be part of In Re: Elmiron MDL No. 2973. Recently, another lawsuit was filed…
Experienced Firm for HawkOne Directional Atherectomy Claims
The FDA has issued a Class 1 recall, which is the most serious kind of recall, for HawkOne Directional Atherectomy Systems. When a Class 1 recall is issued, it is because using the recalled device may cause death or severe injuries. If you were injured or a loved one was…
New Study May Impact Hernia Mesh Claims
Hernia mesh is a medical device commonly placed by surgeons in the area around a hernia in order to support damaged tissue during the healing process. Nine out of 10 hernia surgeries each year involves the mesh. Unfortunately, complications such as bowel obstructions and perforation, sometimes do arise once the…
Recall of Youth All-Terrain Vehicles for Noncompliance with Safety Regulations
On February 2, 2022, certain Maxtrade’s Youth Coolster Mountopz All-Terrain Vehicles (ATVs) were recalled. The recall was issued because the ATVs did not comply with the mandatory federal ATV standard for safety. Notably, youth ATVs didn’t abide by the maximum speed limit for these vehicles when they are meant for…
3M Litigation Update
Military veterans around the United States have sued the manufacturers of 3M Combat Arms Earplugs V2. Their lawsuits allege the earplugs caused the loss of hearing and tinnitus they were supposed to protect against. The litigation came on the heels of the settlement of a whistleblower lawsuit that alleged 3M…
Update on CPAP Litigation
Many people use continuous positive air pressure (CPAP) machines because they have sleep apnea, a common condition. Symptoms of sleep apnea that CPAP machines are meant to address include excessive daytime sleepiness, heavy snoring, memory difficulties and fatigue. When sleep apnea isn’t treated, the result can be depression, diabetes, heart…