Super Cereal Plus fortified corn soya blend, Net Weight 1.5 kg, packaged in a plastic foil bag, packed 9 bags per case
Summary
The FDA issued a Class II for Super Cereal Plus fortified corn soya blend, Net Weight 1.5 kg, packaged in a pl by East Africa Boutique, LLC.. Reason: Products held under insanitary conditions.
Details
Source
Food Recall
External ID
H-0089-2025
Action Date
2025-07-02
Status
Terminated
Category
food
Product Description
Super Cereal Plus fortified corn soya blend, Net Weight 1.5 kg, packaged in a plastic foil bag, packed 9 bags per case
Lot/Code Info: All lot codes and expiration dates for products distributed between 05/06/2025 and 05/12/2025 (exact codes/dates unknown)
Quantity Affected: 19 cases
Reason for Recall
Products held under insanitary conditions
Distribution
Seven (7) retailers in: IN, KY, MO, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-27
Company
Louisville, KY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
East Africa Boutique, LLC. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (East Africa Boutique, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does East Africa Boutique, LLC. have FDA actions?
East Africa Boutique, LLC. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0089-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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