Kabco Recalls Vanilla Powder Distributed in Violation of Consent Decree
Kabco Pharmaceuticals is recalling Perfect 3000 Vanilla Powder because it was distributed in violation of a federal consent decree.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), as they are reasonably likely to cause temporary or medically reversible adverse health consequences.
Plain-English summary
Kabco Pharmaceuticals, Inc. is recalling approximately 1,813.60 kilograms of Perfect 3000 Vanilla Powder, Formula # 3101. The product is a loose powder packaged in bulk drums. The specific lots affected are BA13032004A and 13032004B.
The recall was initiated because the firm distributed the bulk product in violation of the Consent Decree for Permanent Injunction (12-CV-3468). The agency has classified this recall as Class II.
The product was distributed in New York. Consumers and businesses who have this product should stop using it and contact the recalling firm for instructions on how to return or dispose of the product.
The recalled product
- Product
- PERFECT 3000 VANILLA POWDER, FORMULA # 3101. The product is loose powder packaged in bulk drum.
- Manufacturer
- Kabco Pharmaceuticals, Inc.
- Category
- Food — Food Ingredients
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot BA13032004A and 13032004B
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 2 recalled by Kabco Pharmaceuticals, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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