CLASS II Food recall · Reported 16 May 2018 · FDA Enforcement Report
Energique, Dietary Supplement, Enervimin CNCR Focus recalled
Grato Holdings is recalling Energique, Dietary Supplement, Enervimin CNCR Focus, distributed nationwide in the US. The recall was initiated on 16 Apr 2018 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1403-2018
- FDA event ID
- 79774
- Recalling firm
- Grato Holdings, Woodbine, IA
- Brand
- Energique
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 16 Apr 2018
- FDA classified
- 9 May 2018
- Reported
- 16 May 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Hidden Drug Ingredients
- Product category
- Dietary Supplements
Timeline
| 16 Apr 2018 | Recall initiated by company | |
| 9 May 2018 | Classified by FDA | +23 days |
| 16 May 2018 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Multiple products marketed as dietary supplements are unapproved new drugs based on disease claims or routes of administration.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Where it was distributed
Shipped to customers nationwide and Canada.
Questions about this recall
Why was it recalled?
Multiple products marketed as dietary supplements are unapproved new drugs based on disease claims or routes of administration.
Which lots are affected?
50070340, 55837004
Where was it sold?
Shipped to customers nationwide and Canada.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 79774This product is part of a recall event; the main page for the event is Energique, Herbal Supplement, Octocom recalled by Grato Holdings.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Energique, Herbal Supplement, Octocom recalled by Grato HoldingsEnergique | Grato Holdings | Hidden Drug Ingredients | Nationwide | |
| CLASS II | Peaceful Mountain, Nasal Rescue, Dietary Supplement recalledPeaceful Mountain | Grato Holdings | Hidden Drug Ingredients | Nationwide | |
| CLASS II | Peaceful Mountain -Stomach Rescue - Dietary supplement recalledPeaceful Mountain | Grato Holdings | Hidden Drug Ingredients | Nationwide |
More recalls from Grato Holdings
All 18| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | BioActive Nutritional Minaplex, Botanical Herbal Supplement recalledBioActive Nutritional | Grato Holdings | Mold | Nationwide |
| Food | CLASS II | Energique Mineral Magic Dietary Supplement recalled by Grato HoldingsEnergique Mineral | Grato Holdings | Mold | Nationwide |
| Drug | CLASS III | V-force Homeopathic recalled by Grato Holdings | Grato Holdings | Packaging Defects | FL |
| Drug | CLASS II | Earache Drops recalled by Grato HoldingsWalgreens Earache Drops | Grato Holdings | Sterility | Nationwide |
| Drug | CLASS II | Homeopathic EarAche Ear Drops recalled by Grato Holdings | Grato Holdings | Sterility | Nationwide |
Other Dietary Supplements recalls
All 733| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |