Class IITerminated in FDA datasetNov 19, 2025

Shrimp Paste (Klong Kone) 'M'

Recalling firm: GUSTO GROUP, INC.

Why it was recalled

Product tested high for lead.

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The exact product

Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case

Check the codes

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Original FDA code information

DPA159 Shrimp Paste (Klong Kone) 'M'

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.