Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Recalling firm: Progressive Laboratories, Inc
Why it was recalled
Recalled dietary supplements may contain undeclared milk.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 7, 2018.
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ProductXenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
FDA code information
Lot # 2071957 and 2082387
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Full FDA record and distribution details
Original product description
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Original FDA recall reason
Recalled dietary supplements may contain undeclared milk.
Recall details
- Recall number
- F-0915-2018
- Event ID
- 79350
- FDA status
- Terminated
- Initiated
- Feb 23, 2018
- Reported
- Mar 21, 2018
- Classified
- Mar 13, 2018
- Terminated
- Aug 7, 2018
- Quantity
- 147 boxes (2 bottles/box)
- Location
- Irving, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Nationwide through the United States
FDA source record · F-0915-2018
Data updated September 16, 2026. View official FDA data ↗
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