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