Progressive Laboratories product recalled over undeclared milk

Recall date

February 23, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Progressive Laboratories, Inc recalls Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap

Recall number

F-0915-2018

FDA classification

Class I

Brand / firm

Progressive Laboratories, Inc

Sold / distributed

Nationwide through the United States

Why it was recalled

Recalled dietary supplements may contain undeclared milk.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap