Shrimp Paste Recall: Gusto Group Klong Kone L 32 oz Plastic Jar
Announced 2026-01-21 · FDA
FDA is recalling 7 cases of DPA161 Shrimp Paste (Klong Kone) 'L' after testing showed high lead levels. The recalled product was distributed to Iowa (IA) and New Jersey (NJ). Recall number DPA161 Shrimp Paste (Klong Kone) 'L'.
| Brand | GUSTO GROUP, INC. |
|---|---|
| Product | DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases |
| Reason | Product tested high for lead. |
| Severity | moderate |
| Units affected | 7 |
| Distribution | The recalled product was distributed to the following states: IA, NJ |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not eat or use the recalled shrimp paste.
- If you have the product, stop using it and return it to the place of purchase or discard according to local guidelines.
- For instructions or more information, contact the brand or FDA consumer hotline.
How to identify the recalled item
| Lot / date codes | DPA161 Shrimp Paste (Klong Kone) 'L' |
|---|---|
| Lot / date codes | DPA159 Shrimp Paste (Klong Kone) 'M' |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.