Investigations

PPI Medications
Several studies show users experienced heart health issues, including heart attacks, after using PPI medications.
Learn more
Aesculap Knee Replacements
According to the lawsuits, the manufacturer hid problems with its joint replacement implants from regulators, and failed to warn consumers and medical professionals about the increased likelihood of failure.
Learn more
JP Morgan Chase HAMP Loan Modification
Homeowners with mortgages through JPMorgan Chase Bank, N.A. who participated in the HAMP loan modification program should contact us to discuss their participation in the program.
Learn more
Intel Chip Flaw
A security issue was discovered in Intel x86-64x central processing units in 2017 and affects nearly every computer and laptop purchased since 2008, as well as nearly every server installed within that same time period.
Learn more
Medtronic Insulin Pumps
This recall is only the most recent issue related to Medtronic MiniMed Insulin Pumps and involves a malfunction of the infusion set used to supply insulin to diabetic patients.
Learn more
TJI Joists
Homeowners living in houses built after December 2016 with TJI Joists have reported the joists give off a strong “pickled” odor.
Learn more
Hip Replacements
A large percentage of hip replacement failures have been caused due to the design of certain devices with Metal on Metal (MoM) design.
Learn more
Hepatitis C Medications
Concern for the safety of hepatitis C medications is serious enough that the US Food and Drug Administration (FDA) recently issued its strongest warning.
Learn more
Benicar
Seeger Weiss, LLP is investigating claims of users of the drug Benicar who developed serious GI issues including but not limited to: excessive weight loss, vomiting, chronic diarrhea, nausea.
Learn more
Physiomesh
Johnson & Johnson’s Ethicon division issued a full withdrawal in May 2016 concerning its Physiomesh Flexible Composite Mesh. The voluntary withdrawal came after two studies found higher rates of hernia re-opening versus similar products.
Learn more
Invokana
The U.S. Food and Drug Administration has issued a new safety alert regarding a possible increase in the risk of leg or foot amputation after taking the antidiabetic medication, Invokana.
Learn more
Prilosec
While many patients taking this medication were under the impression it would help them with their medical issues, reports have emerged that these patients may be at severe risk for injuries and dangerous side effects.
Learn more
Nexium
Recent research studies have shown an increase in the risk of chronic kidney disease for individuals who take this PPI medication.
Learn more
Onglyza
In 2015, an FDA panel required that AstraZeneca place an additional warning about Onglyza on the label that would warn patients about a potential risk of heart failure.
Learn more
IVC Filter
Complaints about the IVC filters began to surface as early as 2004, but the company continued to sell the devices and did not notify the FDA of complaints or device failures.
Learn more
Testosterone
In 2014, the Food and Drug Administration released a safety announcement warning, telling customers about the potential risks of testosterone therapy.
Learn more
Xarelto
Johnson and Johnson and Bayer AG are currently in the process of settling approximately one dozen lawsuits associated with the blood thinning medication Xarelto.
Learn more
Essure
Investigations have now revealed that Conceptus and Bayer likely knew of the issues with Essure, but failed to warn doctors and users of the device.
Learn more