RecallHawk
Class II Recall

Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169

JINA F&C

Summary

The FDA issued a Class II for Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Pr by JINA F&C. Reason: Product label allergen "contains" statement does not include anchovy(fish).

Details

Source

Food Recall

External ID

H-1221-2026

Action Date

2026-08-12

Status

Ongoing

Category

food

Product Description

Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169

Lot/Code Info: No Lot Codes Used Best by dates: March 28, 2027, June 01, 2027, August 15, 2027, August 25, 2027 and October 15, 2027

Quantity Affected: 4,153 units

Reason for Recall

Product label allergen "contains" statement does not include anchovy(fish)

Distribution

Product is shipped to a distributor's warehouse and distributed through online sales.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-01

Company

JINA F&C

Gyeongju

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 36 food recalls issued in the same week, part of 73 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 (JINA F&C) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JINA F&C have FDA actions?

This is the only FDA action we have on record for JINA F&C in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1221-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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