Class IITerminatedVoluntary: Firm initiated
GUSTO GROUP, INC.: food recall H-0390-2026
GUSTO GROUP, INC. of Paterson, NJ recalled DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases. Reason: Product tested high for lead. The FDA listed it as Class II in its Enforcement Report dated Jan 21, 2026; distribution: Iowa, New Jersey.
Record status as published: Terminated (terminated Apr 7, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
- Product quantity
- 7 cases
- Reason for recall
- Product tested high for lead.
- Codes, lots and dates on the package
- DPA161 Shrimp Paste (Klong Kone) 'L'
- Distribution pattern
- The recalled product was distributed to the following states: IA, NJ
- Recalling firm
- GUSTO GROUP, INC., Paterson, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 19, 2025 |
| Classified by the FDA | Jan 9, 2026 |
| Published in the Enforcement Report | Jan 21, 2026 |
| Terminated | Apr 7, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 98171).
- H-0389-2026 — Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0390-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.