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CriticalFDAfda-F-1673-2024UNDECLARED ALLERGEN

The recalled product is mis-labeled as Ancient Grain + Vegetable Salad item #25247. Product is perishable, refrigerated, and packaged i...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
958
Recall Date
July 3, 2024
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2024.

Undeclared Almond and Soy. The Grain + Celery Salad with Apple Cider Vinaigrette item #47492 was inadvertently mis-labeled as Ancient Grain + Vegetable Salad item #25247. Almond and Soy were not declared on the label of Ancient Grain + Vegetable Salad item #25247.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2024.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Costco Wholesale Corporation or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1673-2024.

Costco Wholesale Corporation

FDA

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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Costco Wholesale Corporation Recall FAQ

Costco Wholesale Corporation is the subject of a produce safety report: The recalled product is mis-labeled as Ancient Grain + Vegetable Salad item #25247. Product is perishable, refrigerated, and packaged i.... The notice was published on July 3, 2024 by the U.S. Food and Drug Administration (FDA). Approximately 958 units are potentially affected.