The Recall Desk
ModerateFDA (Drugs)·D-0576-2016·Announced 2016-01-27

Energique Homeopathic Spray Recalled for Microbial Contamination

Grato Holdings is recalling Energique homeopathic topical spray due to out-of-specification microbial counts. The product was distributed nationwide and to Canada and Guatemala.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate risk of temporary or medically reversible health consequences. The source text does not report any illnesses or injuries, and the hazard is identified as microbial contamination without specific pathogen identification.

Plain-English summary

Grato Holdings, Inc. is recalling 201 bottles of Energique, Homeopathic Remedy, Muscle/Tendon Pain & Stress Relief, Topical Spray, 1 fl oz (30 ml). The product is also labeled as Liddell Laboratories and peaceful mountain Muscle/Tendon Pain & Stress Relief homeopathic spray. The recall involves Lot G9471.

The recall was initiated because testing revealed out-of-specification results for total aerobic microbiological count, indicating microbial contamination of the non-sterile product. The affected units were distributed nationwide and to Guatemala and Canada.

Consumers should stop using the product and return it to the point of purchase or contact the recalling firm for instructions.

The recalled product

Product
Energique, Homeopathic Remedy, Muscle/Tendon Pain & Stress Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0132-1, Dist. by Energique, Inc. Woodbine, IA 51579; ALSO LABELED AS --- Liddell Laboratories, Muscle/Tendon Pain & Stress Relief, Topical Homeopathic Spray, NDC 5
Affected units
201

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot: G9471

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 6 recalled by Grato Holdings, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →