FDA recall record
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 7, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Reason
Product tested high for lead.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Code information listed by FDA
DPA159 Shrimp Paste (Klong Kone) 'M'
Distribution and firm information
Recalling firm listed by FDA: GUSTO GROUP, INC.
Firm location listed by FDA: Paterson, NJ, United States
Distribution reported by FDA: The recalled product was distributed to the following states: IA, NJ
Product quantity listed by FDA: 7 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.