Class ITerminated in FDA datasetRecall initiated Feb 16, 2017

Food City Colby Longhorn Cheese

Why it was recalled

Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes.…

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: Jun 6, 2017.

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ProductFood City Colby Longhorn Cheese, 12 oz. package; also sold in random weight sizes. (Bashas' brand) sold at retail stores) Also sold in 4/13# in Bashas' and Lakeview labels; and RW EW case 36#, no label for Bashas' ;20/1# CW Banquet label and Colby Longhorn Cheese 16 oz. Yokes Fresh Market brand. Banquet is a Lakeview brand name.

Package size12 oz

FDA code information

All product received by Lakeview between September 1, 2016 and January 27, 2017. Lakeview Codes: 1115 Colby LH 4/13#; 1203 Banquet Baby Colby Jk RW Wheel 18/2#; 4355 Colby LH 48/12 oz.; 4358 Longhorn Colby RW EW case 36# No Label; 5536 Colby LH 20/1# CWBanquet Label; 622414 LH Colby 4/13 # R/W - Bahsas'

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Full FDA record and distribution details

Original product description

Food City Colby Longhorn Cheese, 12 oz. package; also sold in random weight sizes. (Bashas' brand) sold at retail stores) Also sold in 4/13# in Bashas' and Lakeview labels; and RW EW case 36#, no label for Bashas' ;20/1# CW Banquet label and Colby Longhorn Cheese 16 oz. Yokes Fresh Market brand. Banquet is a Lakeview brand name.

Original FDA recall reason

Firm was notified by supplier that cheese supplied to Lakeview from September 1, 2016 through January 27, 2017 is being recalled due to the potential of Listeria monocytogenes. contamination.

Recall details

Recall number: F-1661-2017
Event ID: 76549
FDA status: Terminated
Initiated: Feb 16, 2017
Reported: Mar 29, 2017
Classified: Mar 21, 2017
Terminated: Jun 6, 2017
Quantity: 355,477.90 pounds of cheese (all varieties)
Location: Las Vegas, NV, United States
Initiation type: Voluntary: Firm initiated
Notification: E-Mail

Where it was distributed

AZ, CA, UT, NV, WA, OR.

FDA source record · F-1661-2017

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

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