Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Recalled by Gusto Group, INC. on Nov 19, 2025
Recall Summary
Gusto Group, INC. recalled Shrimp Paste (Klong Kone) 'M' in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Nov 19, 2025.
The FDA-published reason for this recall is: "Product tested high for lead."
The product reached multiple states, recorded by the FDA as "The recalled product was distributed to the following states: IA, NJ." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Paterson, NJ. The recall covers 7 cases of product. The FDA has Terminated this recall (first reported Jan 21, 2026), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
Reason for Recall
Product tested high for lead.
Product Description
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case
Distribution
The recalled product was distributed to the following states: IA, NJ
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Browse Related Recalls
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.