Recall Register

Food recall: 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…

Class I FDA enforcement event 89079. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Manufacturer notified US supplier that powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna), on the label.

Class I, in the words of FDA

a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death

J F C International Inc started this food recall on 17 Nov 2021. The firm address in the FDA record is in Commerce, CA. FDA put the recall in Class I. FDA event 89079 has 1 product record. The first FDA enforcement report date is 8 Dec 2021. The record gives the status Terminated, with the termination date 7 Jan 2022.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

HI

Recalling firm

J F C International Inc, Commerce, CA.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 89079: product records
Recall numberProductQuantityClassStatusReport date
F-0231-2022WEL-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,…38 cases & 13,346 EA = 149 cases & 26 EA =17,906 EAClass ITerminated8 Dec 2021

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Food events that started in 2021
463
Share of these events in Class I
35%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
12

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 89079. https://recallregister.com/fda/i/89079/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: HI
What quantity of product is in FDA event 89079?
The FDA record gives this quantity: 38 cases & 13,346 EA = 149 cases & 26 EA =17,906 EA
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2021 have the same class?
35% of the 463 food events that started in 2021 are in Class I.