Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Summary
The FDA issued a Class II for Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ ca by GUSTO GROUP, INC.. Reason: Product tested high for lead..
Details
Source
Food Recall
External ID
H-0389-2026
Action Date
2026-01-21
Status
Terminated
Category
food
Product Description
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Lot/Code Info: DPA159 Shrimp Paste (Klong Kone) 'M'
Quantity Affected: 7 cases
Reason for Recall
Product tested high for lead.
Distribution
The recalled product was distributed to the following states: IA, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-19
Company
Paterson, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
GUSTO GROUP, INC. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GUSTO GROUP, INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GUSTO GROUP, INC. have FDA actions?
GUSTO GROUP, INC. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0389-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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