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High RiskFDAfda-F-1616-2015UNDECLARED ALLERGEN

Organic Sunshine Burgers Gluten Free Soy Free Vegan Loco Chipotle 2 Organic Veggie Burgers Keep Frozen Net WT: 8 OZ. Use By: 8/12/16

Units Affected
780
Recall Date
February 27, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1616-2015.

Gluten testing was performed on products labeled gluten free. The results received back were >20ppm.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1616-2015.

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 Sunshine Burger & Specialty Food Company, Llc 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-1616-2015.

Sunshine Burger & Specialty Food Company, LLC

FDA

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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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📣 Report a food, supplement, or cosmetic problem to the FDA

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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Sunshine Burger & Specialty Food Company, Llc Recall FAQ

Sunshine Burger & Specialty Food Company, Llc is the subject of a snacks & candy safety report: Organic Sunshine Burgers Gluten Free Soy Free Vegan Loco Chipotle 2 Organic Veggie Burgers Keep Frozen Net WT: 8 OZ. Use By: 8/12/16. The notice was published on February 27, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 780 units are potentially affected.