CLASS II Food recall · Reported 2 Aug 2017 · FDA Enforcement Report

Hy-top Rice Mix Chicken Flavored Rice & Vermicelli With Seasonings recalled

Trinidad Benham is recalling Hy-top Rice Mix Chicken Flavored Rice & Vermicelli With Seasonings, distributed in Minnesota, North Carolina, Texas. The recall was initiated on 3 Jul 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes14MAR18L, 18APR18L, 14MAY18L, 15JUN18L
Quantity recalled393 cs/12/6.9 oz boxes

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-2948-2017
FDA event ID
77701
Recalling firm
Trinidad Benham, Denver, CO
Brand
Hy-top
Classification
Class II
Status
Terminated
Recall initiated
3 Jul 2017
FDA classified
27 Jul 2017
Reported
2 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Chicken

Timeline

3 Jul 2017Recall initiated by company
27 Jul 2017Classified by FDA+24 days
2 Aug 2017Published 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

The firm failed to declare wheat in the ingredient statement.

Product as listed by the FDA

HY-TOP Rice MIX CHICKEN FLAVORED RICE & VERMICELLI WITH SEASONINGS NET WT 6.9 OZ (196g)

Where it was distributed

Product was shipped to the following states: MN, NC & TX

MinnesotaNorth CarolinaTexas

Questions about this recall

Why was it recalled?

The firm failed to declare wheat in the ingredient statement.

Which lots are affected?

14MAR18L, 18APR18L, 14MAY18L, 15JUN18L

Where was it sold?

Product was shipped to the following states: MN, NC & TX

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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