In February 2022, manufacturer HRB Brands voluntarily recalled its Sure and Brut Aerosol sprays, which are used as antiperspirants or deodorants to stop or mask body odor. This recall was instituted because benzene, which is carcinogenic, was present in the product. Most of these sprays were distributed in the United…
Reckitt voluntarily recalled certain bottles of 63-count and 75-count Airborne Gummies because it was found that when the bottle is opened for the first time, pressure built up within the bottle presents the possibility of injury. Bottles of gummies that have already been opened do not present this danger to…
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…
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…
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…
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…
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…
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…
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…
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…