Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported January 27, 2016
Energique, 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
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Grato Holdings, Inc. recalled Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bo… - a moderate-severity action.
Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bo… was recalled by Grato Holdings, Inc. in January 27, 2016. Reason: Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aero…. Check the official notice for the remedy. Verify recall #D-0575-2016 with the FDA Drug before acting.
The recall
Grato Holdings, Inc. issued this moderate-severity FDA Drug recall-Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aero….
- Moderate
- severity level
- Class II
- classification
- January 27, 2016
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0575-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0575-2016) was formally reported on January 27, 2016, with the manufacturer initiating the action on December 22, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Grato Holdings, Inc. is listed as the recalling firm, operating out of Woodbine, IA. Federal records list the affected scope as 118 bottles.
The documented reason for this recall is: Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count Distribution data in the federal record shows the product reached: Nationwide and to Guatemala and Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
118 bottles
Related Recalls
6
0 from same agency
Product description
Energique, 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
Reason for recall
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0575-2016 |
| Date reported | January 27, 2016 |
| Date initiated | December 22, 2015 |
| Recalling firm | Grato Holdings, Inc. |
| Firm location | Woodbine, IA |
| Affected scope | 118 bottles |
| Distribution | Nationwide and to Guatemala and Canada. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0575-2016) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Energique, 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. Recalled by Grato Holdings, Inc.. Units affected: 118 bottles.
Why was this product recalled? ▼
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 27, 2016. Severity: Moderate. Recall number: D-0575-2016.
Where was the recalled product distributed? ▼
Distribution: Nationwide and to Guatemala and Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0575-2016) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported January 27, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.