Why it was recalled
Product tested high for lead.
Product description
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Lot numbers, UPCs & expiration codes
DPA159 Shrimp Paste (Klong Kone) 'M'
Where it was sold
The recalled product was distributed to the following states: IA, NJ
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0389-2026
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Nov 19, 2025
- FDA report date
- Jan 21, 2026
- Quantity
- 7 cases
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- GUSTO GROUP, INC.
Original FDA data
Every field from FDA enforcement report H-0389-2026, exactly as published.
Show all FDA fields
- City
- Paterson
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 98171
- Address
- 810 E 27th St
- Code information
- DPA159 Shrimp Paste (Klong Kone) 'M'
- Postal code
- 07513-1215
- Report date
- Jan 21, 2026
- Product type
- Food
- Recall number
- H-0389-2026
- Classification
- Class II
- Recalling firm
- GUSTO GROUP, INC.
- Product quantity
- 7 cases
- Termination date
- Apr 7, 2026
- Reason for recall
- Product tested high for lead.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
- Distribution pattern
- The recalled product was distributed to the following states: IA, NJ
- Recall initiation date
- Nov 19, 2025
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Jan 9, 2026