Check the Batch
Class IITerminated in FDA datasetRecall initiated Aug 22, 2013

Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA#…

Recalling firm: Schafer Fisheries

Why it was recalled

Lack of adequate HACCP records.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 30, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductLabel reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)
Package size24 OZ

FDA code information

Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)

Extracted codes and context

TypeCode / valueContext
lot11945Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/
lot12339Revise8600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12366t Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12367er: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12390Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/201
lot12395rBar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12478Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013
lot12670r: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12694Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8
lot12750Bar Code Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot128158, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.
lot12819de Number: 4278600076; Lot Number: 12478, 11945, 12694, 12390, 12395r, 12750, 12819, 12367, 12339Revise, 12366, 12670, 12815, 12394.; Manufacture date: 7/2/2013, 7/10/2013, 8/13/2013.

Original FDA recall reason

Lack of adequate HACCP records.

Recall details

Recall number
F-0041-2017
Event ID
66278
FDA status
Terminated
Initiated
Aug 22, 2013
Reported
Oct 19, 2016
Classified
Oct 7, 2016
Terminated
May 30, 2018
Quantity
250 cases (12 units per case)
Location
FULTON, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

US: IL, NY, CA

FDA source record · F-0041-2017

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.