Whole Foods Yogurt Cups with Undeclared Almonds Recalled - Food Safety
Whole Food Market recalls single-serve Organic Vanilla Yogurt parfaits with strawberries and granola sold between April 2-11, 2017, due to undeclared almonds. Consumers should check labels for PLU 58260.
Lower-risk recall
Product contains undeclared almonds
Contact the company
What happened, in plain English
Whole Food Market is recalling single-serve Organic Vanilla Yogurt parfait cups with strawberries and granola that were sold between April 2 and April 11, 2017. The product contains undeclared almonds, which could pose a risk for people with nut allergies. Read more at govinfonow.com/recall/21869-whole-foods-yogurt-cups-with-undeclared-almonds-recalled-food-safety.
Source Summary by GovInfoNow · govinfonow.com/recall/21869-whole-foods-yogurt-cups-with-undeclared-almonds-recalled-food-safety · Updated October 8, 2026 · FDA enforcement record: FDA #F-2238-2017
Cite this page
“Whole Foods Yogurt Cups with Undeclared Almonds Recalled - Food Safety.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21869-whole-foods-yogurt-cups-with-undeclared-almonds-recalled-food-safety. Based on FDA recall #F-2238-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2238-2017%22&limit=1).
Why it’s dangerous
The product contains undeclared almonds, meaning it may contain nuts without being labeled as such. This poses a risk for individuals with nut allergies who could experience an allergic reaction if they consume the product.
Who’s affected
People with nut allergies are at risk from this product. The recall applies to consumers who purchased these specific yogurt cups during the listed dates.
How to tell if you have this one
Check for the product name 'Whole Foods single-serve Organic Vanilla Yogurt parfait cups with Strawberries and Granola' and the PLU code 58260. These were sold between April 2 and April 11, 2017.
- Brand
Whole Food Market- Category
Food
What to do — step by step
Check Product Label
Look for the PLU code 58260 on the label to confirm if you have the recalled product.
Where it went and when
Where it was distributed
Distributed in Massachusetts.
FDA distribution: “MA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts.
Recall timeline
FDA terminated this recall 39 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- FDA terminated the recall
- Published in FDA’s Enforcement Report
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 #F-2238-2017 (April 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2238-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.