Stonyfield Organic O'soy Strawberry Yogurt Recall: Undeclared Milk Risk
Stonyfield Farm recalls organic O'soy strawberry yogurt due to potential undeclared milk. Consumers should stop using and check UPC codes 0-52159-00603-7.
Lower-risk recall
Product may contain undeclared milk.
Contact the company
What happened, in plain English
Stonyfield Farm is recalling organic O'soy strawberry yogurt that may contain undeclared milk. This could pose a risk for people with milk allergies. The product was sold from November 2017. Read more at govinfonow.com/recall/20334-stonyfield-organic-o-soy-strawberry-yogurt-recall-undeclared-milk-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20334-stonyfield-organic-o-soy-strawberry-yogurt-recall-undeclared-milk-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0132-2018
Cite this page
“Stonyfield Organic O'soy Strawberry Yogurt Recall: Undeclared Milk Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20334-stonyfield-organic-o-soy-strawberry-yogurt-recall-undeclared-milk-risk. Based on FDA recall #F-0132-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0132-2018%22&limit=1).
Why it’s dangerous
The yogurt may contain undeclared milk, which can cause allergic reactions in sensitive individuals. This is a food safety issue that requires careful checking of ingredients.
Who’s affected
People with milk allergies are most at risk from this yogurt recall. Anyone who purchased the product with UPC code 0-52159-00603-7 is affected.
How to tell if you have this one
Check for the UPC code 0-52159-00603-7 on the product label. The product is Stonyfield Organic O'soy Strawberry on the bottom SOY YOGURT 5.3 Oz (150g).
- Brand
Stonyfield Farm- Product
Stonyfield ORGANIC O'soy Strawberry on the bottom SOY YOGURT 5.3 Oz (150g), UPC Codes: 0-52159-00603-7. KEEP- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 0-52159-00603-7 on the yogurt container.
Where it went and when
Where it was distributed
Distributed in 18 states.
FDA distribution: “CA, CT, FL, IA, IL, MA, MD, ME, MI, NC, NH, NJ, NY, OH, PA, SC, VA, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Connecticut, Florida, Illinois, Iowa, Maine, Maryland, Massachusetts, Michigan, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 35 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is there a deadline to act?
The recall was issued on November 4, 2017, but there is no specific deadline mentioned in the official notice.
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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-0132-2018 (October 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0132-2018 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.