FDA recall record
Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
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 February 1, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
Reason
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
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.
Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
Code information listed by FDA
unknown
Distribution and firm information
Recalling firm listed by FDA: Luckyberry
Firm location listed by FDA: Lawrence, KS, United States
Distribution reported by FDA: To retailers in Lawrence, KS.
Product quantity listed by FDA: At least 5 bottles
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.