FDA recall record
ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml
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 24, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml
Reason
Non-compliance with process authority schedule; temperature at start of thermal process not recorded.
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.
ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml
Code information listed by FDA
070320
Distribution and firm information
Recalling firm listed by FDA: Root 23 LLC
Firm location listed by FDA: Columbus, OH, United States
Distribution reported by FDA: Distributed to the states of AZ, CA, CO, CT, GA, IL, KS, LA, MA, MI, NJ, NM, NY, OH, OR, PA, TX, WV. No sales to foreign countries or government agencies/DoD.
Product quantity listed by FDA: 390 Units
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.