Severity
Moderate
FDA Food recall · Reported March 7, 2018
The firm was notified by The Ohio Dept. of Agriculture that their products contained dietary and health claims.
The recall
Divine Living issued this moderate-severity FDA Food recall — The firm was notified by The Ohio Dept. of Agriculture that their products contained dietary and health claim….
Sourced from official FDA Food enforcement records. Verify recall #F-0876-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0876-2018) was formally reported on March 7, 2018, with the manufacturer initiating the action on January 22, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Divine Living is listed as the recalling firm, operating out of West Unity, OH. Federal records list the affected scope as 20/3/8oz & 17/2oz bottles.
The documented reason for this recall is: The firm was notified by The Ohio Dept. of Agriculture that their products contained dietary and health claims. Distribution data in the federal record shows the product reached: Product was shipped to the following states: AZ, OH & TX. 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, 5 from FDA Food — 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.
Where this recall sits in its category — 711 dietary supplements recalls on record
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Severity
Moderate
Affected scope
20/3/8oz & 17/2oz bottles
Related Recalls
6
5 from same agency
Divine Living Silver with harmonically structured frequencies A Wellness Solution 8 oz Ingredients: Structured Water, Pure Silver West Unity, Ohio 419-682-0918
The firm was notified by The Ohio Dept. of Agriculture that their products contained dietary and health claims.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0876-2018 |
| Date reported | March 7, 2018 |
| Date initiated | January 22, 2018 |
| Recalling firm | Divine Living |
| Firm location | West Unity, OH |
| Affected scope | 20/3/8oz & 17/2oz bottles |
| Distribution | Product was shipped to the following states: AZ, OH & TX |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported March 7, 2018.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).