Class IITerminated in FDA datasetAug 22, 2013

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

Recalling firm: Schafer Fisheries

Why it was recalled

Lack of adequate HACCP records.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original 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.

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.

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.