Signature Cafe Sandwich Philly Cheesesteak hot and cold;regular and large sizes. All Signature Cafe Made to o

Recall map → All recalls → F-1914-2012

Signature Cafe Sandwich Philly Cheesesteak hot and cold;regular and large sizes. All Signature Cafe Made to order sandwiches for which customers asked for optional green Pepper and yellow onion mix. Manufactured by GH Foods CA LLC, Rancho Cordova, CA. GH Foods CA LLC · reported 2012-08-15

Terminated This recall has been closed out by the agency.

Reason for recall: GH Foods CA received notification from Gills onions of a recall of onions due to Listeria Monocytogenes. GH Foods used the recalled onions in numerous product.
Classification: Class I
Recall initiated: 2012-07-26
Reported by the agency: 2012-08-15
Closed out (terminated): 2013-01-31
Recalling firm: GH Foods CA LLC
Sacramento, CA
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): CA, NV, AZ, UT, AZ, CO, NM, SD, WY, NE.
States we parsed from that text: AZ CA CO NE NM NV SD UT WY
The agency named these states. Parse method explicit_state_list, confidence high.
Food category: Prepared meals & entrees Produce (fruit & vegetables)derived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1914-2012

Verifying this record. Everything above is FDA's own record, reproduced. FDA publishes no web page for an individual enforcement report, so the only direct link is the machine-readable one:

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To look it up yourself, search recall number F-1914-2012 in FDA's Enforcement Report. That search cannot be linked to directly, so the number has to be pasted in.

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.