FDA recall record
PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
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 March 9, 2016. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
Reason
Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468).
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.
PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
Code information listed by FDA
Lot BA13032004A and 13032004B
Distribution and firm information
Recalling firm listed by FDA: Kabco Pharmaceuticals, Inc.
Firm location listed by FDA: Amityville, NY, United States
Distribution reported by FDA: New York
Product quantity listed by FDA: 1813.60 Kilograms
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.