Class ITerminated in FDA datasetRecall initiated Nov 20, 2016

FRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich,…

Recalling firm: LSG Sky Chefs, Inc.

Why it was recalled

Mediterranean Chicken with Hummus ready to eat sandwich, refrigerated product, is recalled due to a potential contamination with Listeria monocytogenes. The sandwich contains the…

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: Jan 18, 2017.

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ProductFRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich, refrigerated, packed in plastic clam shell, net wt. 8 oz. The UPC is 0 52548 58888 5.
Package size8 oz

FDA code information

Best By 11/19/2016 (production date 11/17/2016) Best By 11/20/2016 (production date 11/18/2016) Best By 11/21/2016 (production date 11/19/2016)

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Full FDA record and distribution details

Original product description

FRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich, refrigerated, packed in plastic clam shell, net wt. 8 oz. The UPC is 0 52548 58888 5.

Extracted codes and context

TypeCode / valueContext
best by11/19/2016Best By 11/19/2016 (production date 11/17/2016) Best By 11/20/2016 (production date 11/18/2016) Best By 11/21/2016 (production date 11/1
best by11/20/2016Best By 11/19/2016 (production date 11/17/2016) Best By 11/20/2016 (production date 11/18/2016) Best By 11/21/2016 (production date 11/19/2016)
best by11/21/2016tion date 11/17/2016) Best By 11/20/2016 (production date 11/18/2016) Best By 11/21/2016 (production date 11/19/2016)

Original FDA recall reason

Mediterranean Chicken with Hummus ready to eat sandwich, refrigerated product, is recalled due to a potential contamination with Listeria monocytogenes. The sandwich contains the affected Roasted Red Pepper Hummus which was recalled by Sabra Dipping Co., LLC.

Recall details

Recall number
F-0750-2017
Event ID
75779
FDA status
Terminated
Initiated
Nov 20, 2016
Reported
Dec 21, 2016
Classified
Dec 15, 2016
Terminated
Jan 18, 2017
Quantity
103 pieces
Location
Seattle, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in Oregon and Washington

FDA source record · F-0750-2017

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

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