FDA recall record
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags;...
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 April 25, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags; 2) Krasdale Onion Rings, NET WT 16 OZ, packaged in plastic bags; 3) Spartan Onion Rings, NET WT 20 OZ, packaged in plastic bags; 4) Shur Fine Onion Rings, NET WT. 16 OZ, packaged in plastic bags; 5) Kroger Onion Rings, NET WT.
20 OZ, packaged in plastic bags; and 6) Fareway Breaded Onion Rings, NET WT. 20 OZ, packaged in plastic bags.
Reason
Product label does not declare milk.
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.
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags; 2) Krasdale Onion Rings, NET WT 16 OZ, packaged in plastic bags; 3) Spartan Onion Rings, NET WT 20 OZ, packaged in plastic bags; 4) Shur Fine Onion Rings, NET WT. 16 OZ, packaged in plastic bags; 5) Kroger Onion Rings, NET WT.
20 OZ, packaged in plastic bags; and 6) Fareway Breaded Onion Rings, NET WT. 20 OZ, packaged in plastic bags.
Code information listed by FDA
Product manufactured after October 20, 2015 and prior to September 23, 2016 with production date codes: V151020 through V160923.
Distribution and firm information
Recalling firm listed by FDA: McCain Foods USA
Firm location listed by FDA: Lisle, IL, United States
Distribution reported by FDA: Recalled product was distributed to direct accounts in AL, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NY, OH, TN, TX, VA, and WI
Product quantity listed by FDA: 1) 29,956 cases; 2) 1,318 cases; 3) 5,087 cases; 4) 4,313 cases; 5) 16,440 cases; 6) 2,200 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.