Nootri Toto food product recalled due to insanitary conditions
East Africa Boutique, LLC is recalling Nootri Toto (1 kg packages) distributed to seven retailers in Indiana, Kentucky, Missouri, and Ohio due to products being held under insanitary conditions.
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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall for a condition (insanitary storage) that creates a potential for adverse health consequences but with no reported illnesses or injuries, making it a precautionary action typical of a Moderate severity classification.
Plain-English summary
East Africa Boutique, LLC is recalling Nootri Toto, a food product sold in 1 kg packages and packaged in cardboard boxes, due to insanitary storage conditions. The recalled products were distributed between May 6, 2025 and May 12, 2025 to seven retailers located in Indiana, Kentucky, Missouri, and Ohio.
Consumers who have purchased Nootri Toto during this distribution period should not consume the product. Anyone with questions or concerns should contact East Africa Boutique, LLC or consult with their healthcare provider.
The recalled product
- Product
- Nootri Toto, Net Weight 1 kg, packaged in a cardboard box, packed 12 boxes per case
- Manufacturer
- East Africa Boutique, LLC.
- Category
- Food
- Hazard
- Affected units
- 2
Distribution
Part of a larger recall action
This product is one of 2 recalled by East Africa Boutique, LLC. 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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