Product labeling is on the bottom of the container. Label reads in part "SMALL HEART STRAWBERRY TRAY WITH DEVONSHIRE DIP***Use By: 02/16...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1410-2015.
Real Foods of Seattle, LLC discovered that the wrong dressing was added to the package of strawberries. The wrong dressing contains egg and soy, which is not declared on the product packaging.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1410-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Real Foods Of Seattle, Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-1410-2015.
Real Foods of Seattle, LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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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.
Real Foods Of Seattle, Llc Recall FAQ
Real Foods Of Seattle, Llc is the subject of a produce safety report: Product labeling is on the bottom of the container. Label reads in part "SMALL HEART STRAWBERRY TRAY WITH DEVONSHIRE DIP***Use By: 02/16.... The notice was published on February 10, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 356 units are potentially affected.