Why it was recalled
The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
Product description
RegenErect
Lot numbers, UPCs & expiration codes
all lots
Where it was sold
US
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-1820-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Mar 9, 2017
- FDA report date
- Apr 12, 2017
- Quantity
- unknown
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- VivaCeuticals, Inc. dba Regeneca Worldwide
Original FDA data
Every field from FDA enforcement report F-1820-2017, exactly as published.
Show all FDA fields
- City
- Irvine
- State
- CA
- Status
- Terminated
- Country
- United States
- Event ID
- 76634
- Address
- 2 Park Plaza
- Address (line 2)
- Suite 1200
- Code information
- all lots
- Postal code
- 92614-2562
- Report date
- Apr 12, 2017
- Product type
- Food
- Recall number
- F-1820-2017
- Classification
- Class II
- Recalling firm
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Product quantity
- unknown
- Termination date
- Aug 8, 2017
- Reason for recall
- The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- RegenErect
- Distribution pattern
- US
- Recall initiation date
- Mar 9, 2017
- Initial firm notification
- Press Release
- Center classification date
- Mar 31, 2017