Boba Direct Taro Powder Recalled for Undeclared Allergens
Boba Direct, Inc. is recalling taro flavored powder due to undeclared allergens. The product was distributed in five US states.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves allergen mislabeling on common allergens, which corresponds to a High severity score under the rubric.
Plain-English summary
Boba Direct, Inc. is recalling foil bags containing 2.2 lbs. of taro flavored powder sold under the Boba Direct, Inc. brand. The recall is being conducted because the product contains undeclared allergens. The product code is TaroPwdr-BD, and all lots are affected.
The affected product was distributed in Illinois, Missouri, Ohio, Florida, and Tennessee. The U.S. Food and Drug Administration has classified this recall as Class II.
Consumers who have purchased this product should stop using it and contact Boba Direct, Inc. for further instructions or a refund.
The recalled product
- Product
- Foil bags containing 2.2 lbs. each of taro flavored powder and sold under the Boba Direct, Inc. brand.
- Manufacturer
- Boba Direct, Inc.
- Category
- Food — Powders / Flavorings
- 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 (2)
- Product code: TaroPwdr-BD
- All lots
Distribution
Part of a larger recall action
This product is one of 24 recalled by Boba Direct, 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.
See all 24 products in this recall →Related recalls
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