Monfefo brand Turmeric Shot — Class II food recall F-0860-2021
Terminated recall by Monfefo LLC, reported 2021-08-18, distributed in CA, CO, CT, DC, FL, GA, MA, MD…. Product was not manufactured according to specifications.
| Recall number | F-0860-2021 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Monfefo LLC, Brooklyn, NY, United States |
| Recall initiated | 2021-07-26 |
| Classified | 2021-08-11 |
| Reported by FDA | 2021-08-18 |
| Terminated | 2022-05-23 |
| Distributed | CA, CO, CT, DC, FL, GA, MA, MD, ME, NC, NJ, NY, OH, PA, SC, TX, VA, VT, WI |
| Quantity | 25 cases |
| UPC / GTIN / UDI-DI | 00860002515410 |
| Lot numbers | 1792126, 1882127, 1942128 |
| Expiration dates | 2021-08-17 |
Product
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Reason for recall
Product was not manufactured according to specifications.
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-0860-2021. 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.