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Use caution Drug recall · FDA · Published December 22, 2015

Energique Homeopathic Spray Recall: Microbial Contamination

Grato Holdings recalls Energique homeopathic skin spray due to microbial contamination. Check lot G9471 for details on this Class II recall.

🇺🇸 FDA recall #D-0575-2016DrugEnergique ›
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Recalling firmGrato Holdings, Inc.201 Apple Blvd · Woodbine, IA 51579-1503
✎ GovInfoNow plain-language explainer

What happened, in plain English

Grato Holdings, Inc. is recalling Energique Homeopathic Remedy, Skin Irritant & Healing Support Topical Spray because it contains microbial contamination. The product was found to have out-of-specification total aerobic microbiological counts during testing. This recall affects approximately 118 bottles distributed nationwide and to Canada and Guatemala. Read more at govinfonow.com/recall/43311-energique-homeopathic-spray-recall-microbial-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/43311-energique-homeopathic-spray-recall-microbial-contamination · Updated October 11, 2026 · FDA enforcement record: FDA #D-0575-2016

Cite this page

“Energique Homeopathic Spray Recall: Microbial Contamination.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43311-energique-homeopathic-spray-recall-microbial-contamination. Based on FDA recall #D-0575-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0575-2016%22&limit=1).

Why it’s dangerous

The topical spray is non-sterile but failed testing for total aerobic microbiological count, meaning it contains higher-than-allowed levels of bacteria or other microbes. Applying contaminated products to the skin can lead to infection or adverse reactions, particularly if the skin barrier is compromised.

Who’s affected

Consumers who purchased the recalled Energique homeopathic skin spray, specifically those with lot number G9471. Individuals using the product for skin irritation or healing support are at risk of exposure to microbial contamination.

How to tell if you have this one

Check your bottle for the brand name Energique (also labeled as Peaceful Mountain or Liddell Laboratories) and the lot number G9471. Verify the NDC numbers: 44911-0136-1, 50845-0214-1, or 43846-0046-1. The product is a 1 fl oz topical spray.

  • Brand
    Energique
  • Product
    Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bottle, NDC 44911-0136-1, Dist
  • Category
    Drug
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide and to Guatemala and Canada.
Recall numberProduct, codes & lotsQuantity
D-0575-2016Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bottle, NDC 44911-0136-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Skin Irritant & Healing Support, Topical Homeopathic Spray, NDC 50845-0214-1, Dist By Liddell Laboratories, Inc., Woodbine, IA; and peaceful mountain, skin irritant & healing support, homeopathic spray, UPC 8 18692 00880 4, NDC 43846-0046-1, Dist. by Peaceful Mountain, Inc. Woodbine, IA; Lot: G9471118 bottles
D-0576-2016Energique, 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 50845-0219-1, Dist By Liddell Laboratories, Inc., Woodbine, IA; and peaceful mountain, Muscle/Tendon Pain & Stress Relief, homeopathic spray, UPC 8 18692 00870 5, NDC 43846-0043, Dist. by Peaceful Mountain, Inc. Woodbine, IA; Lot: G9471201 bottles
D-0577-2016Energique, Homeopathic Remedy, Joint Pain & Stiffness Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0133-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Joint Pain & Stiffness Relief, Topical Homeopathic Spray, NDC 50845-0218-1, Dist By Liddell Laboratories, Inc., Woodbine, IA; and peaceful mountain, Joint Pain & Stiffness Relief, homeopathic spray, UPC 8 18692 00890 3, NDC 43846-0042-1, Dist. by Peaceful Mountain, Inc. Woodbine, IA; Lot: G9471224 bottles
D-0578-2016Energique, 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; Lot: G9471371 bottles
D-0579-2016Energique, 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; Lot: G947190 bottles
D-0580-2016Energique, Homeopathic Remedy, First Aid Pain & Trauma Relief, 1 fl oz (30 ml) bottles, NDC 44911-0135-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, First Aid Pain & Trauma Relief, Topical Homeopathic Spray, NDC 50845-0216-1, Dist By Liddell Laboratories, Inc., Woodbine, IA; and peaceful mountain, First Aid Pain & Trauma Relief, homeopathic spray, UPC 8 18692 00895 8, NDC 43846-0045-1, Dist. by Peaceful Mountain, Inc. Woodbine, IA; Lot: G9471118 bottles
Based on the official FDA remedy

What to do — step by step

  1. Stop Using the Product

    Cease use of the Energique homeopathic skin spray immediately due to microbial contamination risks.

  2. Check Your Lot Number

    Verify if your bottle has lot number G9471 and one of the specified NDC or UPC codes.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide and to Guatemala and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 15 months after the firm started it.

1. Firm started the recall: Dec 22, 201512. FDA classified it Class II: Jan 20, 201623. Published in FDA’s Enforcement Report: Jan 27, 201634. FDA terminated the recall: Mar 10, 2017420152017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0575-2016 (December 22, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0575-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA