FDA Recall United States Terminated Historical recordClass II
J F C International Inc
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- Distribution
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J F C International Inc Recall: Manufacturer notified US supplier that powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna), on the label.
United States
TerminatedClass I
- Company
- J F C International Inc
- Product
- WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock;…
- Recall date
- November 17, 2021
- Terminated
- January 7, 2022
- Source
- FDA
Reason for recall
Manufacturer notified US supplier that powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna), on the label.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152 83660 7 Product of Japan; Imported by JFC International Inc., Los Angeles, CA 90040 INGREDIENTS: SALT, MONOSODIUM GLUTAMATE, SUGAR, GLUCOSE, SHRIMP EXTRACT POWDER (TAPIOCA, SWEET POTATO, CORN, SHRIMP, MONOSODIUM GLUTAMATE, SALT, BEET, SOYBEAN, DISODIUM SUCCINATE), SHRIMP POWDER, CORN OIL, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, CITRIC ACID, MIXED SEASONING (MONOSODIUM GLUTAMATE, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, HYDROLYZED PROTEIN (CORN, WHEAT, SOYBEAN, TAPIOCA), DEXTRIN, SALT, SUGAR, POTATO STARCH). CONTAINS: CRUSTACEAN SHELLFISH (SHRIMP), SOYBEAN, WHEAT | Not published in this source record | 38 cases & 13,346 EA = 149 cases & 26 EA =17,906 EA | All lots |
Distribution
- HI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0231-2022
- Event ID
- 89079
- Status
- Terminated
- Classification
- Class I
- Company
- J F C International Inc
- Product description
- WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152 83660 7 Product of Japan; Imported by JFC International Inc., Los Angeles, CA 90040 INGREDIENTS: SALT, MONOSODIUM GLUTAMATE, SUGAR, GLUCOSE, SHRIMP EXTRACT POWDER (TAPIOCA, SWEET POTATO, CORN, SHRIMP, MONOSODIUM GLUTAMATE, SALT, BEET, SOYBEAN, DISODIUM SUCCINATE), SHRIMP POWDER, CORN OIL, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, CITRIC ACID, MIXED SEASONING (MONOSODIUM GLUTAMATE, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, HYDROLYZED PROTEIN (CORN, WHEAT, SOYBEAN, TAPIOCA), DEXTRIN, SALT, SUGAR, POTATO STARCH). CONTAINS: CRUSTACEAN SHELLFISH (SHRIMP), SOYBEAN, WHEAT
- Quantity
- 38 cases & 13,346 EA = 149 cases & 26 EA =17,906 EA
- Reason
- Manufacturer notified US supplier that powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna), on the label.
- Recall initiation date
- November 17, 2021
- Report date
- December 8, 2021
- Classification date
- Not published in this source record
- Termination date
- January 7, 2022
- Distribution pattern
- HI
- UPC, lot, and code information
- All lots
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: J F C International Inc
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- Product
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- Published
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- Distribution
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A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Hawaii | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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