CLASS II Food recall · Reported 16 May 2018 · FDA Enforcement Report

Energique, Herbal Supplement, Octocom recalled by Grato Holdings

Grato Holdings is recalling Energique, Herbal Supplement, Octocom, 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

Lot, batch or date codesJ20597, J20840, J21846, J21849, J21850, J23464, J23465, J23466, J23467
Quantity recalled845 1-oz bottles, 59 1-oz bottles

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-1401-2018
FDA event ID
79774
Recalling firm
Grato Holdings, Woodbine, IA
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
Product category
Herbal Supplements

Timeline

16 Apr 2018Recall initiated by company
9 May 2018Classified by FDA+23 days
16 May 2018Published 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, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579

Where it was distributed

Shipped to customers nationwide and Canada.

Nationwide

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?

J20597, J20840, J21846, J21849, J21850, J23464, J23465, J23466, J23467

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 79774

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