Food Recall Check
Class III · Low risk Terminated Initiated Jan 17, 2013 (14 years ago)

Tausi Brand Salted Black Beans recall

Recalled by Walong Marketing, Inc. · Buena Park, CA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Walong is recalling Tausi Brand Salted Black Beans because it may have the potential for pathogen growth and toxin formation due to Clostridium botulinum or other spoilage organisms.

Pathogen: Botulism

Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.

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

Tausi Brand Salted Black Beans, 180g (6.34oz), 100 cans/carton This product is in a two piece can with a single seam. This 6.34 oz can is wrapped with a label containing, red, yellow, and black text labeled in part "Tausi Brand Salted Black Beans***Distributed by: V8 Commercial Co, Inc. San Juan, Metro Manila Produc of the Phillipines***Ingredients: Black Beans, water, Iodized salt, sugar and caramel Net wt. 180g(6.34oz)**BB:___"

Quantity: 650 cartons

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 lots

Where it was sold

Nationwide.

FDA's distribution note: nationwide

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
Walong Marketing, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 17, 2013
In FDA report of
Mar 20, 2013
Terminated
Nov 8, 2013
FDA recall number
F-1132-2013 · event 35779
Official record
FDA enforcement report search

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