Skip to main content
High RiskFDAfda-F-1648-2014UNDECLARED ALLERGEN

Nicomex Color Para Tamal Net Wt 1/8 oz (3.54gms) Productos Mexicanos Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055 Tel....

Category
Units Affected
93
Recall Date
December 7, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1648-2014.

Nicomex Inc. is recalling Camaron Entero for undeclared sulfites and Color Para Tamal for unapproved color based on NYSDAM Laboratory analysis.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1648-2014.

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 Nicomex 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-1648-2014.

Nicomex 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

Nicomex Inc. Recall FAQ

Nicomex Inc. is the subject of a food safety report: Nicomex Color Para Tamal Net Wt 1/8 oz (3.54gms) Productos Mexicanos Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055 Tel..... The notice was published on December 7, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 93 units are potentially affected.