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FDA recall 99358: JINA F&C: Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium…

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FDARecall 99358Food

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Product label allergen "contains" statement does not include anchovy(fish)
Text from FDA, unedited.

FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.

Is it yours? Products and codes

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

    Lot or code
    No Lot Codes Used Best by dates: March 28, 2027, June 01, 2027, August 15, 2027, August 25, 2027 and October 15, 2027
    FDA recall number
    H-1221-2026
    Quantity
    4,153 units

Distribution (FDA): Product is shipped to a distributor's warehouse and distributed through online sales.

About this record

Issued by
U.S. Food and Drug Administration
Firm
JINA F&C
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Product label allergen "contains" statement does not include anchovy(fish)”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99358 on August 12, 2026.

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