Shrimp Paste (Klong Kone) 'M'
Recalling firm: GUSTO GROUP, INC.
Why it was recalled
Product tested high for lead.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 7, 2026.
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ProductShrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Package size16 oz
FDA code information
DPA159 Shrimp Paste (Klong Kone) 'M'
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Full FDA record and distribution details
Original product description
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Original FDA recall reason
Product tested high for lead.
Recall details
- Recall number
- H-0389-2026
- Event ID
- 98171
- FDA status
- Terminated
- Initiated
- Nov 19, 2025
- Reported
- Jan 21, 2026
- Classified
- Jan 9, 2026
- Terminated
- Apr 7, 2026
- Quantity
- 7 cases
- Location
- Paterson, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
The recalled product was distributed to the following states: IA, NJ
FDA source record · H-0389-2026
Data updated September 16, 2026. View official FDA data ↗
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