CLASS II Food recall · Reported 13 Jan 2016 · FDA Enforcement Report

Velitas Candies Candles Net recalled by Nicomex

Nicomex is recalling Nicomex Velitas Candies Candles Net, distributed in New Jersey, New York. The recall was initiated on 23 Nov 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC 884678102323
Quantity recalled316 packages (2 ounce units)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0467-2016
FDA event ID
72826
Recalling firm
Nicomex, Passaic, NJ
Classification
Class II
Status
Terminated
Recall initiated
23 Nov 2015
FDA classified
7 Jan 2016
Reported
13 Jan 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Candy

Timeline

23 Nov 2015Recall initiated by company
7 Jan 2016Classified by FDA+45 days
13 Jan 2016Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

This recall has been initiated because the laboratory analysis indicates that the product contains FD & C Red #3, and Yellow #5 which are not declared on the ingredient statement on the product label.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Nicomex Velitas Candies Candles Net. Wt. 2 oz (56.7 gms) Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055

Where it was distributed

NJ and NY.

New JerseyNew York

Questions about this recall

Is Velitas Candies Candles Net recalled?

Yes. Nicomex recalled Velitas Candies Candles Net on 23 Nov 2015. The recall is Class II and its status is Terminated. Recall number F-0467-2016.

Why was it recalled?

This recall has been initiated because the laboratory analysis indicates that the product contains FD & C Red #3, and Yellow #5 which are not declared on the ingredient statement on the product label.

Which lots are affected?

UPC 884678102323

Where was it sold?

NJ and NY.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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