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Progressive Laboratories, Inc
FDA recall F-0915-2018 · Class I · reported 2018-03-21 · Terminated
- Product
- Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Quantity
- 147 boxes (2 bottles/box)
- Distribution
- Nationwide through the United States
- Firm location
- TX, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Press Release
- Recall started
- 2018-02-23
- Terminated
- 2018-08-07
- Code info
- Lot # 2071957 and 2082387
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.