Key Points<\/p>\n
Nephronex liquid multivitamins were recalled in 24 states due to contamination with black particles.<\/p>\n
The recall affects bottles with lot code “B2025” and expiration date “08\/27.”<\/p>\n
The FDA classified this as a Class II recall; health risks are minor, but seek care if concerns arise.<\/p>\n
There\u2019s an active recall on a dietary supplement sold in 24 states, according to the U.S. Food and Drug Administration (FDA). Over 4,000 units of product are affected due to a foreign matter contamination .<\/p>\n
Per the California State Board of Pharmacy\u2019s alert, the specific supplement recalled is Nephronex multivitamin supplement. The multivitamin contained vitamin b-complex, vitamin c and folic acid, and were sold in 8-fluid-ounce bottles in the following states: 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.<\/p>\n
The recalled product has a printed lot code of \u201cB2025\u201d and expiration date \u201c08\/27\u201d printed on its bottle. Check your liquid multivitamin, and if you have the matching recalled item on hand, dispose of it or return to your place of purchase for a potential refund. The recalled vitamins could have been purchased as early as February 2026 through May.<\/p>\n
According to the FDA, the recall was issued due to a \u201cforeign object\u201d found in the supplements, specifically \u201cblack particulate matter.\u201d On May 19, this alert was classified as a Class II recall, meaning consuming the liquid multivitamin may lead to minor, temporary health problems. Seek medical attention if you are experiencing any health concerns.<\/p>\n
For further questions about this recall, contact the FDA by calling 1-888-INFO-FDA (1-888-463-6332).<\/p>\n