Skip to main content
High RiskFDAfda-F-2785-2015OTHER

Sunridge Candy-Coconut Chews, Vanilla. 10 lb. box. Item code: 023617; UPC: 086700936177 Falcon Trading Company Inc/Sun Ridge Farms,...

Units Affected
156
Recall Date
May 22, 2015
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2785-2015.

Firm noticed stainless steel wire fragments, approximately .2 MM in diameter and between 1 to 3 inches in length in shredded coconut received from supplier in Sri Lanka.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2785-2015.

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 Falcon Trading Co., 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-2785-2015.

Falcon Trading Co., 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.

Visit FDA.gov →

📣 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.

How to report to FDAFile a report at FDA

Falcon Trading Co., Inc. Recall FAQ

Falcon Trading Co., Inc. is the subject of a snacks & candy safety report: Sunridge Candy-Coconut Chews, Vanilla. 10 lb. box. Item code: 023617; UPC: 086700936177 Falcon Trading Company Inc/Sun Ridge Farms,.... The notice was published on May 22, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 156 units are potentially affected.