PERFECT 3000 VANILLA POWDER — Class II food recall F-1767-2013
Terminated recall by Kabco Pharmaceuticals, Inc., reported 2013-08-07, distributed in NY. Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468)
| Recall number | F-1767-2013 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Kabco Pharmaceuticals, Inc., Amityville, NY, United States |
| Recall initiated | 2013-04-09 |
| Classified | 2013-07-30 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2016-03-09 |
| Distributed | NY |
| Quantity | 1,813.6 kilograms |
| Lot numbers | 13032004B, BA13032004A |
Product
PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
Reason for recall
Firm had distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468).
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-1767-2013. 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.