A liquid multivitamin supplement sold across 24 states and territories has been recalled due to contamination concerns, federal regulators announced.
Recall Details
The U.S. Food and Drug Administration classified the action as a Class II recall on Tuesday, citing the potential presence of a “black particulate matter” or “foreign object.” A Class II classification means that consuming the affected product could cause temporary or medically reversible adverse health effects.
The recall, initiated by Miami-based Llorens Pharmaceuticals International Division, Inc., involves more than 4,000 units of Nephronex multivitamin supplement. This is an 8-fluid-ounce liquid formula containing vitamin B-complex, vitamin C, and folic acid. According to a consumer alert from the California State Board of Pharmacy, the affected bottles carry the lot code “B2025” and an expiration date of “08/27.”
States Affected
Regulators stated the product was sold between February 2026 and May 2026 in the following states and territories: Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Massachusetts, Minnesota, Missouri, New Jersey, New York, North Carolina, Ohio, Oklahoma, Puerto Rico, Tennessee, Texas, Virginia, Washington, West Virginia, and Wisconsin.
Consumer Advice
Health officials advise consumers who have the matching product to stop using it immediately. The items should be discarded or returned to the place of purchase for a refund. Individuals experiencing health concerns after taking the supplement are urged to seek medical attention.
Consumers seeking additional details regarding the recall can contact the FDA directly at 1-888-463-6332.
The Independent has reached out to Llorens Pharmaceuticals for comment.
