CLASS II Food recall · Reported 21 Oct 2015 · FDA Enforcement Report

Glutinous Rice recalled by Win Luck Trading

Win Luck Trading is recalling Glutinous Rice, distributed in New Jersey. The recall was initiated on 14 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes881168
Quantity recalled80 cases (12 bottles per case)

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-0009-2016
FDA event ID
71932
Recalling firm
Win Luck Trading, Bayonne, NJ
Classification
Class II
Status
Terminated
Recall initiated
14 Jul 2015
FDA classified
13 Oct 2015
Reported
21 Oct 2015
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Allergens
Product category
Rice

Timeline

14 Jul 2015Recall initiated by company
13 Oct 2015Classified by FDA+91 days
21 Oct 2015Published in enforcement report+8 days

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

Reason for recall

Win Luck is recalling Grove Grow Notes Glutinous Rice because it contains undeclared alcohol.

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

Glutinous Rice, Net WT. 1000 g, packaged in plastic bottles, UPC 6958020881168, Made in China

Where it was distributed

NJ

New Jersey

Questions about this recall

Why was it recalled?

Win Luck is recalling Grove Grow Notes Glutinous Rice because it contains undeclared alcohol.

Which lots are affected?

881168

Where was it sold?

NJ

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 26 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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