Luckyberry Cold-Pressed Juice — Class II food recall F-0766-2019
Terminated recall by Luckyberry, reported 2018-12-26, distributed in KS. The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Jui
| Recall number | F-0766-2019 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Luckyberry, Lawrence, KS, United States |
| Recall initiated | 2018-10-30 |
| Classified | 2019-01-30 |
| Reported by FDA | 2018-12-26 |
| Terminated | 2019-02-01 |
| Distributed | KS |
| Quantity | 3 bottles |
Product
Luckyberry Cold-Pressed Juice, NoCoast, Kale, Cucumber, Green Apple, Celery, Lemon, Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
Reason for recall
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0766-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.