The Center for Disease Control and Prevention (CDC) estimates that 500 thousand to one million people who lived and worked at Camp Lejeune Military base were exposed to toxic elements in the water supply between 1953 and 1987.
The Camp Lejeune Justice Act was enacted in 2022, enabling those who suffered from exposure to the toxic waters of Camp Lejeune, to file claims against responsible parties including the U.S.
CaseyGerry is investigating reports linking the use of the prescription drug Ozempic® to Cholelothiasis (gallstones), Cholecystitis (inflammation of the gallbladder), and other gallbladder health issues, as well as Gastroparesis.
Ozempic® and similar medications are used by some patients with diabetes to control blood glucose levels.
SAN DIEGO (June 6, 2023) Frederick Schenk, a longtime CaseyGerry partner and head of the firm’s mass torts practice, was recently appointed by Judge Carolyn Kuhl of the Los Angeles Superior Court to serve on the plaintiffs steering committee in the social media judicial council coordination proceedings (JCCP) lawsuit against some of the world’s biggest Social media companies, including Facebook and Instagram, YouTube, SnapChat, TikTok, and others.
Boppy has re-issued a recall of the Boppy Infant Lounger which has been linked to at least 10 infant deaths. The Boppy loungers under recall are the Boppy Original Newborn Loungers, Boppy Preferred Newborn Loungers and Pottery Barn Kids Boppy Newborn Loungers.
CaseyGerry partner and head of Mass torts, Frederick Schenk has been appointed to the Plaintiffs Steering Committee in the Social Media Judicial Council Coordination Proceedings (JCCP) lawsuit against several of the world’s biggest Social media companies, including Facebook and Instagram, YouTube, SnapChat, TikTok, and others.
In the fall of 2022, CaseyGerry alerted consumers to the Exactech®, recall for knee and ankle replacement implants due to the early degradation of the polyethylene liner used in these medical implants.
Global medical device company, Exactech, has issued a recall for knee and ankle replacement implants. The recall has affected at least 250,000 individuals.
According to Drugwatch, the Florida-based company, which has been manufacturing implants such as joint replacements since 1985, issued the recall due to potential degradation of the polyethylene liner in ankle and knee joints caused by improper packaging.
