FDA recall record
All American Cheeseburger Product ID 470007
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of May 31, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
All American Cheeseburger Product ID 470007
Reason
Potential Listeria monocytogenes contamination.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
All American Cheeseburger Product ID 470007
Code information listed by FDA
Lot #051916B, 060916D
Distribution and firm information
Recalling firm listed by FDA: Let's Do Lunch, Inc.
Firm location listed by FDA: Gardena, CA, United States
Distribution reported by FDA: U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.
Product quantity listed by FDA: 207 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.