Why it was recalled
Recalled dietary supplements may contain undeclared milk.
Product description
Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
Lot numbers, UPCs & expiration codes
Lot # 2071887
Where it was sold
Nationwide through the United States
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0914-2018
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Feb 23, 2018
- FDA report date
- Mar 21, 2018
- Quantity
- 88 boxes (2 bottles/box)
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Progressive Laboratories, Inc
Original FDA data
Every field from FDA enforcement report F-0914-2018, exactly as published.
Show all FDA fields
- City
- Irving
- State
- TX
- Status
- Terminated
- Country
- United States
- Event ID
- 79350
- Address
- 3131 Story Rd W
- Code information
- Lot # 2071887
- Postal code
- 75038-3514
- Report date
- Mar 21, 2018
- Product type
- Food
- Recall number
- F-0914-2018
- Classification
- Class I
- Recalling firm
- Progressive Laboratories, Inc
- Product quantity
- 88 boxes (2 bottles/box)
- Termination date
- Aug 7, 2018
- Reason for recall
- Recalled dietary supplements may contain undeclared milk.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
- Distribution pattern
- Nationwide through the United States
- Recall initiation date
- Feb 23, 2018
- Initial firm notification
- Press Release
- Center classification date
- Mar 13, 2018