Nicomex Candy Mex, Productos Mexicanos, Distributed by Nicomex, Inc., 88 First Street, Passaic, NJ 07055
⚠ 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-1918-2015.
Nicomex Inc. is recalling Candy Mex Candy Coated Nuts because the product tested positive for almonds, peanuts, FD&C Red #3, FD&C Red #40, FD&C Yellow #5 and FD&C Blue #1. This product also did not have an ingredient listing label.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1918-2015.
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 Nicomex Inc. 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-1918-2015.
Nicomex Inc.
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.
Nicomex Inc. Recall FAQ
Nicomex Inc. is the subject of a snacks & candy safety report: Nicomex Candy Mex, Productos Mexicanos, Distributed by Nicomex, Inc., 88 First Street, Passaic, NJ 07055. The notice was published on February 27, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 24 units are potentially affected.