ALOHA VANILLA PREMIUM PROTEIN is a powder and product is packed as the following: 1) Tin:
Recalling firm: Aloha
Why it was recalled
Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin
The exact product
ALOHA VANILLA PREMIUM PROTEIN is a powder and product is packed as the following: 1) Tin: UPC 641061842606, 2) Pouch: UPC 641061842644 and 3) Protein Tower 14 pack: UPC 640864820729. Formulated, Quality Tested & Exclusively Sold by ALOHA, Inc. NY, NY 10011 +1 888.444.3898
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
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Original FDA code information
All lot codes (GI-6940, GI-6967, GI-7009, GI-7039)
| Type | Code / value | Context |
|---|---|---|
| UPC | 640864820729 | UPC 641061842606, 2) Pouch: UPC 641061842644 and 3) Protein Tower 14 pack: UPC 640864820729. Formulated, Quality Tested & Exclusively Sold by ALOHA, Inc. NY, NY 10011 +1 888.444.3898 |
| UPC | 641061842606 | PREMIUM PROTEIN is a powder and product is packed as the following: 1) Tin: UPC 641061842606, 2) Pouch: UPC 641061842644 and 3) Protein Tower 14 pack: UPC 640864820729. Formulated, Quality Tested & Exclusively S |
| UPC | 641061842644 | and product is packed as the following: 1) Tin: UPC 641061842606, 2) Pouch: UPC 641061842644 and 3) Protein Tower 14 pack: UPC 640864820729. Formulated, Quality Tested & Exclusively Sold by ALOHA, Inc. NY, NY 10 |
Recall details
- Recall number
- F-1587-2015
- Event ID
- 70398
- FDA status
- Terminated
- Initiated
- Jan 29, 2015
- Reported
- Apr 1, 2015
- Classified
- Mar 24, 2015
- Terminated
- May 3, 2017
- Quantity
- 58,146 units
- Location
- New York, NY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
nationwide via internet sales and in NY via 6 retail stores.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.