Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Recalling firm: Grato Holdings, Inc.
Multiple products marketed as dietary supplements are unapproved new drugs based on disease claims or routes of administration.
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 17, 2018.
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FDA code information
50070340, 55837004
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Full FDA record and distribution details
Original product description
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Original FDA recall reason
Multiple products marketed as dietary supplements are unapproved new drugs based on disease claims or routes of administration.
Recall details
- Recall number
- F-1403-2018
- Event ID
- 79774
- FDA status
- Terminated
- Initiated
- Apr 16, 2018
- Reported
- May 16, 2018
- Classified
- May 9, 2018
- Terminated
- Aug 17, 2018
- Quantity
- 767 120-tablet bottles
- Location
- Woodbine, IA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Shipped to customers nationwide and Canada.
Data updated September 16, 2026. View official FDA data ↗
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