Shrimp Paste (Klong Kone) 'M'
Reason Product tested high for lead.
DPA161 Shrimp Paste recall
Recalled by Gusto Group, INC. · Paterson, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product tested high for lead.
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
Quantity: 7 cases
Food: Seafood & fish
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
DPA161 Shrimp Paste (Klong Kone) 'L'
Where it was sold
Iowa New Jersey
FDA's distribution note: The recalled product was distributed to the following states: IA, NJ
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Gusto Group, INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 19, 2025
- In FDA report of
- Jan 21, 2026
- Terminated
- Apr 7, 2026
- FDA recall number
- H-0390-2026 · event 98171
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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