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.
The exact product
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot # 2071957 and 2082387
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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.