J F C International Inc Recall: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab. - F-0803-2018
🇺🇸 United States
TerminatedClass I
Company
J F C International Inc
Product
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per…
Recall date
February 1, 2018
Terminated
April 12, 2018
Source
FDA
Reason for recall
Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported by JFC International Inc., Los Angeles, CA.
Not published in this source record
2563 cases and 3 pouches
All lots
Distribution
CA
NV
WA
OR
UT
AK
AZ
TX
OK
OH
MO
KY
MI
WI
NE
IL. IN
KS
NY
CT
NJ
PA
MA
MD
DE
DC
VA
HI.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0803-2018
Event ID
79106
Status
Terminated
Classification
Class I
Company
J F C International Inc
Product description
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported by JFC International Inc., Los Angeles, CA.
Quantity
2563 cases and 3 pouches
Reason
Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.
Recall initiation date
February 1, 2018
Report date
February 14, 2018
Classification date
Not published in this source record
Termination date
April 12, 2018
Distribution pattern
CA, NV, WA, OR, UT, AK, AZ, TX, OK, OH, MO, KY, MI, WI, NE, IL. IN, KS, NY, CT, NJ, PA, MA, MD, DE, DC, VA, HI.
UPC, lot, and code information
All lots
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
California
1
Nevada
1
Washington
1
Oregon
1
Utah
1
Alaska
1
Arizona
1
Texas
1
Oklahoma
1
Ohio
1
Missouri
1
Kentucky
1
Michigan
1
Wisconsin
1
Nebraska
1
Illinois
1
Indiana
1
Kansas
1
New York
1
Connecticut
1
New Jersey
1
Pennsylvania
1
Massachusetts
1
Maryland
1
Delaware
1
District of Columbia
1
Virginia
1
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.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of April 12, 2018.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
Read the full medical disclaimer.