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High RiskFDAfda-F-0025-2016UNDECLARED ALLERGEN

Caravelle ABC Cookies Banh Chu NET WT: 7oz (200gr) Product of Vietnam

Units Affected
25
Recall Date
August 14, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0025-2016.

Anhing Corporation is recalling Caravelle ABC Cookies because recent analysis revealed each cookie contained a lead level of 0.13 ppm and 13 ppm per labeled serving size. In addition the label did not declare flour as wheat flour, and stated the product contained vegetable oil when it was refined coconut oil.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0025-2016.

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 Anhing 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-0025-2016.

Anhing Corporation

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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Anhing Corporation Recall FAQ

Anhing Corporation is the subject of a bakery & grains safety report: Caravelle ABC Cookies Banh Chu NET WT: 7oz (200gr) Product of Vietnam. The notice was published on August 14, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 25 units are potentially affected.