FDA recall record
RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
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 September 29, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
Reason
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
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.
RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
Code information listed by FDA
Mixed Berry, single bar, UPC 57777 00467, 12-count carton, UPC 57777 00470, 4-count carton, UPC 59162 00700 Best By Dates between 3/14/2019 5/6/2019 and 7/10/2019 8/30/2019
Distribution and firm information
Recalling firm listed by FDA: CHICAGO BAR COMPANY LLC RXBAR
Firm location listed by FDA: Chicago, IL, United States
Distribution reported by FDA: Domestic:AL, AR, AZ,CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI Foreign: The firm did not report any foreign distribution DOD: NV, VA
Product quantity listed by FDA: 75,695,266 Individually wrapped bars
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.