CLASS II Food recall · Reported 21 Jan 2026 · FDA Enforcement Report

DPA161 Shrimp Paste (Klong Kone) 'L' , 12 packages / cases recalled

Gusto Group is recalling DPA161 Shrimp Paste (Klong Kone) 'L' , 12 packages / cases, distributed in Iowa, New Jersey. The recall was initiated on 19 Nov 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDPA161 Shrimp Paste (Klong Kone) 'L'
Quantity recalled7 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0390-2026
FDA event ID
98171
Recalling firm
Gusto Group, Paterson, NJ
Brand
Dpa161
Classification
Class II
Status
Terminated
Recall initiated
19 Nov 2025
FDA classified
9 Jan 2026
Reported
21 Jan 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Lead & Heavy Metals
Product category
Shrimp

Timeline

19 Nov 2025Recall initiated by company
9 Jan 2026Classified by FDA+51 days
21 Jan 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product tested high for lead.

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases

Where it was distributed

The recalled product was distributed to the following states: IA, NJ

IowaNew Jersey

Questions about this recall

Why was it recalled?

Product tested high for lead.

Which lots are affected?

DPA161 Shrimp Paste (Klong Kone) 'L'

Where was it sold?

The recalled product was distributed to the following states: IA, NJ

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 98171

This product is part of a recall event; the main page for the event is Shrimp Paste (Klong Kone) 'M' , 24 packages/ case recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIShrimp Paste (Klong Kone) 'M' , 24 packages/ case recalledGusto GroupLead & Heavy MetalsIA, NJ

More recalls from Gusto Group

All 2
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIShrimp Paste (Klong Kone) 'M' , 24 packages/ case recalledGusto GroupLead & Heavy MetalsIA, NJ

Other Shrimp recalls

All 144