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
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
- Brand
- Nicomex Velitas
- 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 2015 | Recall initiated by company | |
| 7 Jan 2016 | Classified by FDA | +45 days |
| 13 Jan 2016 | Published 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.
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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