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Why Regulators Recalled Some Valsartan Products
In 2018, the U.S. Food and Drug Administration announced recalls of select valsartan medications after laboratory testing detected NDMA in pills produced by specific overseas manufacturers.
These recalls did not affect every valsartan product. The FDA limited the action to certain lots and suppliers and continues to monitor manufacturers for compliance with safety standards.
Patients who took valsartan may wish to confirm whether their prescription appeared on a recall list.
Carabin Law is currently reviewing claims involving recalled valsartan products and the potential health effects associated with their use.
What Is NDMA?
NDMA is a chemical byproduct that can form during some industrial and pharmaceutical manufacturing processes. People may encounter small amounts of NDMA in food, water, or the environment. However, regulators raised concern when the substance appeared in medication meant for daily, long-term use.
Because patients rely on blood pressure drugs for ongoing treatment, even low-level contamination can raise serious safety questions.
Health Concerns Raised in Legal Claims
Some individuals who used recalled valsartan products later reported serious health conditions. Legal claims often involve concerns related to:
Liver injury
Liver scarring or fibrosis
Liver tumors
Liver cancer
Medical outcomes differ from person to person. A diagnosis alone does not prove that a medication caused the condition. Attorneys and medical professionals review each situation individually before drawing conclusions.
Injured? Contact Carabin Law
If you took a recalled valsartan medication and later experienced serious liver-related health issues, you may want to explore your legal options.
Our attorneys are evaluating paraquat-related claims and can explain potential legal options during a free, confidential consultation.