Klong Kone: Klong Kone Shrimp Paste — FDA announcement Jan 8, 2026

Reported terminated

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Jan 8, 2026. 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
Klong Kone Shrimp Paste
Reason
Potential Metal Contaminant - Lead
Classification
Not supplied
Recalling firm
Gusto Group Inc.
Quantity
Not supplied
Agency-reported status
Terminated in FDA listing
Source record identifier
ad0cb8129ca5610f

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicability[Klong Kone] Shrimp Paste (Klong Kone) '454 G. (1 LBS)' , with UPC: 8853142000313, Product Code: DPA159; [Klong Kone] Shrimp Paste (Klong Kone) '910 G. (2 LBS)' , with UPC: 8853142000320, Product Code: DPA161; To date, there has been one report of four children becoming ill, which involved diarrhea and elevated blood levels. This recall was initiated following this report of illness associated with consumption of the product. The FDA collected product samples from retail locations and lab analysis found that the finished products contained elevated levels of lead. The company has ceased distribution of this lot. The company is currently investigating the cause of the issue.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

The recalled product was directly distributed to the two retailers listed below, located IA and NJ , between April 2023 to December 2023 There were no online sales. The recalled [Klong Kone] Shimp Paste (Klong Kone) “454 G. (1 LBS)” and “910 G. (2 LBS),” is packaged in a white plastic jar with a red cap. The product is a dark-colored paste with a salty flavor. The product was Packed and Distributed By: P. Prateepthong 2000, Product of Thailand. The recalled product was sold in two sizes:

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Jan 8, 2026
Company announcement date
Jan 8, 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.

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