FDA recall record
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
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 May 23, 2022. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Reason
Product was not manufactured according to specifications.
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.
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Code information listed by FDA
Turmeric Shot 12 pack: UPC 660002515441 Turmeric Shot single shot: UPC 860002515410 LOTS: 1942128; 1882127; 1792126 EXP: 8/17/21; 8/23/21; 9/14/21; 9/21/21
Distribution and firm information
Recalling firm listed by FDA: Monfefo LLC
Firm location listed by FDA: Brooklyn, NY, United States
Distribution reported by FDA: NY, NJ, CT, TX, MD, DC, FL, ME, MA, VT, OH, PA, VA, GA, NC, SC, WI, CO, CA
Product quantity listed by FDA: 25 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.