FDA recall H-0390-2026 · Jan 21, 2026
GUSTO GROUP, INC.: DPA161 Shrimp Paste (Klong Kone) 'L' recall
Product
DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
Reason for recall
Product tested high for lead.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- DPA161 Shrimp Paste (Klong Kone) 'L'
- Quantity
- 7 cases
- Distribution
- The recalled product was distributed to the following states: IA, NJ
- Recalling firm
- GUSTO GROUP, INC., Paterson, NJ
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-11-19
Source: openFDA enforcement record H-0390-2026 · search recall number H-0390-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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