Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Dec 22, 2015 (11 years ago)

Energique

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

Energique, Homeopathic Remedy, Headache Pain & Sinus Pressure Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0134-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Headache Pain & Sinus Pressure Relief, Topical Homeopathic Spray, NDC 50845-0217-1, Dist By Liddell Laboratories, Inc., Woodbine, IA 51579; and peaceful mountain, Headache Pain & Sinus Pressure Relief, homeopathic spray, UPC 8 18692 00885 9, NDC 43846-0041-1, Dist. by Peaceful Mountain, Inc. Woodbine, IA

Affected NDCs 43846-0041-01 44911-0134-01 50845-0217-01

Compare with the code on your package — it is the most precise check available.

Recalling firm
Grato Holdings, Inc.
NDC code
44911-0134-1
Origin
IA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0579-2016 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Grato Holdings, Inc.

All 2015 recalls
Class III · Low risk

V-FORCE Homeopathic

Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).

Terminated cGMP deviation Grato Holdings, Inc. D-0099-2024
Class II · Moderate risk

Earache Drops

Microbial contamination of non-sterile product.

Terminated Microbial contamination Grato Holdings, Inc. NDC 0363-3233-15 D-0991-2022

Other microbial contamination recalls from 2015

All microbial contamination recalls
Class II · Moderate risk

Energique

Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count

Terminated Microbial contamination Grato Holdings, Inc. NDC 44911-0135-1 D-0580-2016
Class II · Moderate risk

Energique

Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count

Terminated Microbial contamination Grato Holdings, Inc. NDC 44911-0137-1 D-0578-2016
Class II · Moderate risk

Energique

Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count

Terminated Microbial contamination Grato Holdings, Inc. NDC 44911-0133-1 D-0577-2016
Class II · Moderate risk

Energique

Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count

Terminated Microbial contamination Grato Holdings, Inc. NDC 44911-0132-1 D-0576-2016