RecallHawk
Class II Recall

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container

FDMR, INC DBA SUJI'S KOREAN CUISINE

Summary

The FDA issued a Class II for Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master ca by FDMR, INC DBA SUJI'S KOREAN CUISINE. Reason: Hazelnuts were declared in ingredient statement but not in Contains statement..

Details

Source

Food Recall

External ID

F-0898-2022

Action Date

2022-03-23

Status

Terminated

Category

food

Product Description

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean Cuisine, Seattle, WA Country of Origin: Republic of Korea.

Lot/Code Info: All lots

Quantity Affected: 63,451sold

Reason for Recall

Hazelnuts were declared in ingredient statement but not in Contains statement.

Distribution

Nationwide to wholesale customer locations in AK, AL,AR,AZ,CA,CO,CT,DC, DE,FL, GA, HI,IA, ID, IL, IN, KS, KY,LA,MA,MD, MI, MN, MO, MS, MT, NA, NC, ND,NE, NH, NJ, NM, NV, NY, OH,OK,OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-17

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (FDMR, INC DBA SUJI'S KOREAN CUISINE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does FDMR, INC DBA SUJI'S KOREAN CUISINE have FDA actions?

This is the only FDA action we have on record for FDMR, INC DBA SUJI'S KOREAN CUISINE in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0898-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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