Recall archive / FDA food enforcement
DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases — FDA record H-0390-2026
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 19, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
- Reason
- Product tested high for lead.
- Classification
- Class II
- Recalling firm
- GUSTO GROUP, INC.
- Quantity
- 7 cases
- Agency-reported status
- Terminated
- Source record identifier
- H-0390-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | DPA161 Shrimp Paste (Klong Kone) 'L' |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
The recalled product was distributed to the following states: IA, NJ
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 21, 2026
- Recall initiation date
- Nov 19, 2025
- Center classification date
- Jan 9, 2026
- Termination date
- Apr 7, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.