Severity
Moderate
The recall
Nicomex Inc. issued this moderate-severity FDA Food recall — This recall has been initiated because the laboratory analysis indicates that the product contains FD & C Red….
Sourced from official FDA Food enforcement records. Verify recall #F-0467-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0467-2016) was formally reported on January 13, 2016, with the manufacturer initiating the action on November 23, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Nicomex Inc. is listed as the recalling firm, operating out of Passaic, NJ. Federal records indicate 316 packages (2 ounce units) units are affected.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: NJ and NY.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.
Severity
Moderate
Units Affected
316 packages (2 ounce units)
Related Recalls
6
0 from same agency
Nicomex Velitas Candies Candles Net. Wt. 2 oz (56.7 gms) Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0467-2016 |
| Date reported | January 13, 2016 |
| Date initiated | November 23, 2015 |
| Recalling firm | Nicomex Inc. |
| Units affected | 316 packages (2 ounce units) |
| Distribution | NJ and NY. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Learn how the US recall system works and how to protect yourself and your household.
How the US Recall System Works
The three federal agencies, how recalls are initiated, and what happens next.
Understanding Recall Severity Classes
What Class I, II, and III mean and which recalls demand immediate action.
What to Do When a Product Is Recalled
Verify, claim your remedy, report injuries, and navigate the process.
How to Check If Your Products Are Recalled
Step-by-step guide to checking food, products, medications, and vehicles.
Recalled Products in Your Home
A room-by-room household audit guide for active recalls.
Most Recalled Product Categories
Rankings of highest-recall categories from FDA, CPSC, and NHTSA.
Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
Keep tracking product safety across the federal recall archive.
Recall Checker
Search the full archive by product name, brand, or recall number across every agency.
Check a product →
FDA Food recalls
Every recall issued by FDA Food, newest first.
Browse the feed →
RecallRadar
Live feed of the latest recalls across the FDA, CPSC and NHTSA — filter by agency and severity.
View the live feed →
Rankings
The largest recalls by units affected and the most-recalled product categories.
See the rankings →
Browse by category
Find recalls by product type to spot recurring defect patterns.
All categories →
What to do next
A step-by-step guide to refunds, repairs, and returns after a recall.
Read the guide →
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
Electrolux Consumer Products, Inc., of Charlotte, North Carolina · 2026-03-19
· 2026-03-19
· 2026-03-19
· 2026-02-26
Jiangsu Ever-Tie Lighting Co., Ltd, of China · 2026-02-26
Compare this recall with Electrolux Group Recalls Frigidaire Gas Ranges Due to Burn … →
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 13, 2016.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).