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Lower risk Food recall · FDA · Published January 22, 2018

Divine Living Silver Wellness Solution 8oz Product Contains Unverified Health Claims

Divine Living recalls 8oz Silver Wellness Solution products for containing unverified health claims. The Ohio Department of Agriculture notified the firm of dietary and health claims violations.

🇺🇸 FDA recall #F-0876-2018FoodDivine Living ›
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Recalling firmDivine Living20675 County Road I50 · West Unity, OH 43570-9519
✎ GovInfoNow plain-language explainer

What happened, in plain English

Divine Living is recalling their Silver Wellness Solution 8oz products because they contain health claims that the Ohio Department of Agriculture found unverified. This means the product's health benefits are not supported by evidence. Read more at govinfonow.com/recall/19736-divine-living-silver-wellness-solution-8oz-product-contains-unverified-health.

Source Summary by GovInfoNow · govinfonow.com/recall/19736-divine-living-silver-wellness-solution-8oz-product-contains-unverified-health · Updated October 7, 2026 · FDA enforcement record: FDA #F-0876-2018

Cite this page

“Divine Living Silver Wellness Solution 8oz Product Contains Unverified Health Claims.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19736-divine-living-silver-wellness-solution-8oz-product-contains-unverified-health. Based on FDA recall #F-0876-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0876-2018%22&limit=1).

Why it’s dangerous

The product makes health claims that the Ohio Department of: Agriculture found unverified. This means the product's health benefits are not supported by evidence. The hazard is not a physical risk but a violation of health claim regulations.

Who’s affected

Anyone who purchased Divine Living's Silver Wellness Solution 8oz products. People most at risk are those who rely on these products for health benefits.

How to tell if you have this one

Look for Divine Living Silver Wellness Solution 8oz products with ingredients listed as Structured Water, Pure Silver. These were sold starting from January 22, 2018.

  • Brand
    Divine Living
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Review the product label for the 8oz Silver Wellness Solution with Structured Water and Pure Silver ingredients.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Product was shipped to the following states: AZ, OH & TX” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Ohio, Texas.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Jan 22, 201812. FDA classified it Class II: Mar 1, 201823. Published in FDA’s Enforcement Report: Mar 7, 201834. FDA terminated the recall: Jul 11, 201842018
  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.

✎ GovInfoNow

Questions people ask

What should I do if I have this product?

The recall does not require immediate action; check the product label to confirm if it matches the recalled items.

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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 #F-0876-2018 (January 22, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0876-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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