Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 29, 2015 (12 years ago)

ALOHA CHOCOLATE PREMIUM PROTEIN is a powder and recall

Recalled by Aloha · New York, NY, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin

Pathogen: Staphylococcus

Staph bacteria that can produce heat-stable toxins.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

ALOHA CHOCOLATE PREMIUM PROTEIN is a powder and , product is packed as the following: 1) Tin: UPC 641061842613, 2) Pouch: UPC 641061842651 and 3) Protein Tower 14 pack: UPC 640864820743. Formulated, Quality Tested & Exclusively Sold by ALOHA, Inc. NY, NY 10011 +1 888.444.3898

Quantity: 49,658 units

Food: Chocolate & candy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

All codes (GH-6934, GH-6981, GH-7008, GH-7038)

Where it was sold

Nationwide.

New York

FDA's distribution note: nationwide via internet sales and in NY via 6 retail stores.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Aloha
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 29, 2015
In FDA report of
Apr 1, 2015
Terminated
May 3, 2017
FDA recall number
F-1588-2015 · event 70398
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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