Shrimp Paste recall
Recalled by GUSTO GROUP, INC.
The product, as the FDA describes it: Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Why it was recalled
Product tested high for lead.
The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.
What to do if you have it
The agency has published the reason above without naming a health hazard class of its own. Match your package against the codes below, and when it matches, return it rather than deciding for yourself whether it looks fine.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
DPA159 Shrimp Paste (Klong Kone) 'M'
The details on record
| Recalling company | GUSTO GROUP, INC. |
|---|---|
| Company location | Paterson, NJ |
| Where it was distributed | The recalled product was distributed to the following states: IA, NJ |
| How much was recalled | 7 cases |
| Recall started | November 19, 2025 |
| Published by the FDA | January 21, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| FDA recall number | H-0389-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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