Energique — Class II drug recall D-0578-2016

Terminated recall by Grato Holdings, Inc., reported 2016-01-27, distributed nationwide. Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerob

Recall number	`D-0578-2016`
Product type	Drug
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Grato Holdings, Inc., Woodbine, IA, United States
Recall initiated	2015-12-22
Classified	2016-01-20
Reported by FDA	2016-01-27
Terminated	2017-03-10
Distributed	Nationwide (US)
Countries outside the US	CA, GT
Quantity	371 bottles
Reason classes	microbial contamination, sterility, specification failure
UPC / GTIN / UDI-DI	`00818692008750`
NDC	`43845-0044-01`, `44911-0137-01`, `50845-0215-01`
Lot numbers	`G9471`

Product

Energique, Homeopathic Remedy, Shingles Pain & Ulceration Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0137-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Shingles Pain & Ulceration Relief Topical Homeopathic Spray, NDC 50845-0215-1, Dist By Liddell Laboratories, Inc., Woodbine, IA 51579; and peaceful mountain, Shingles Pain & Ulceration Relief, homeopathic spray, UPC 8 18692 00875 0, NDC 43845-0044-1, Dist. by Peaceful Mountain, Inc. Woodbine, IA

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0578-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.