CLASS II Food recall · Reported 12 Aug 2020 · FDA Enforcement Report

Khaotan Rice Cracker recalled by Siam Trading

Siam Trading is recalling Khaotan Rice Cracker, distributed in 11 states. The recall was initiated on 13 Jul 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesall codes or best by dates
Quantity recalled50 cases

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-1144-2020
FDA event ID
86064
Recalling firm
Siam Trading, Brooklyn, NY
Brand
Khaotan
Classification
Class II
Status
Terminated
Recall initiated
13 Jul 2020
FDA classified
6 Aug 2020
Reported
12 Aug 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Tree Nuts
Product category
Crackers

Timeline

13 Jul 2020Recall initiated by company
6 Aug 2020Classified by FDA+24 days
12 Aug 2020Published 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

Mae Bua Jun/Khaotan Rice Cracker contains visible cashews that are not declared.

Product as listed by the FDA

Khaotan Rice Cracker, Net Wt. 150g

Where it was distributed

NY, VA, NC, OH, IN, WI, MN, IL, PA, IA, NE

IowaIllinoisIndianaMinnesotaNorth CarolinaNebraskaNew YorkOhioPennsylvaniaVirginiaWisconsin

Questions about this recall

Is Khaotan Rice Cracker recalled?

Yes. Siam Trading recalled Khaotan Rice Cracker on 13 Jul 2020. The recall is Class II and its status is Terminated. Recall number F-1144-2020.

Why was it recalled?

Mae Bua Jun/Khaotan Rice Cracker contains visible cashews that are not declared.

Which lots are affected?

all codes or best by dates

Where was it sold?

NY, VA, NC, OH, IN, WI, MN, IL, PA, IA, NE

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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