FDA recall record
A&W Cream Soda 12 FL OZ (355 mL)
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 December 4, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
A&W Cream Soda 12 FL OZ (355 mL)
Reason
The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the statement "caffeine free" and the product contains caffeine
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.
A&W Cream Soda 12 FL OZ (355 mL)
Code information listed by FDA
Lot Codes: G5184VE and G5195VE
Distribution and firm information
Recalling firm listed by FDA: Dr. Pepper Snapple Group Inc
Firm location listed by FDA: Plano, TX, United States
Distribution reported by FDA: U.S. distribution to the following; CA, NV, and ID. No foreign consignees.
Product quantity listed by FDA: 10,292 cases (12 cans/case)
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.