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CriticalFDAfda-F-1113-2018UNDECLARED ALLERGEN

EXO Cricket Protein Bar Apple Cinnamon; Net Wt. 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000014

⚠ 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
20,000
Recall Date
March 16, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1113-2018.

Products contain undeclared sulfites

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1113-2018.

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 Aspire Food Group Usa Inc. 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-1113-2018.

Aspire Food Group USA Inc.

FDA

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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📣 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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Aspire Food Group Usa Inc. Recall FAQ

Aspire Food Group Usa Inc. is the subject of a food safety report: EXO Cricket Protein Bar Apple Cinnamon; Net Wt. 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000014. The notice was published on March 16, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 20,000 units are potentially affected.