Aloha — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Aloha has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 29 Jan 2015. Aloha is categorized under Snacks & Candy based on their predominant recall history.
Recall activity over time for Aloha
How serious are Aloha recalls?
FDA recall classifications by severity
Full FDA recall history for Aloha
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 29 Jan 2015Official FDA Notice | ALOHA VANILLA PREMIUM PROTEIN is a powder and product is packed as the following: 1) Tin: UPC 641061842606, 2) Pouch: UP | Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin | Class IITerminated |
| 29 Jan 2015Official FDA Notice | ALOHA CHOCOLATE PREMIUM PROTEIN is a powder and , product is packed as the following: 1) Tin: UPC 641061842613, 2) Pouch | Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin | Class IITerminated |
| 29 Jan 2015Official FDA Notice | ALOHA VANILLA AND CHOCOLATE PREMIUM PROTEIN powders are distributed under the following labels: 1) ALOHA PREMIUM PROTEI | Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin | Class IITerminated |
Where have Aloha recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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