← FDA ENFORCEMENT
H-0390-2026Class II
GUSTO GROUP, INC.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
GUSTO GROUP, INC.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2026-01-21
Distribution
The recalled product was distributed to the following states: IA, NJ
Firm state
NJ
Product quantity
7 cases
Initiated by
Voluntary: Firm initiated
Reason for recall
Product tested high for lead.
Product description
DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
Code / lot info
DPA161 Shrimp Paste (Klong Kone) 'L'
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →