Tausi Brand Salted Black Beans recall
Recalled by Golden Dharma International Corp · Rowland Heights, CA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Golden Dharma International 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: 910 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.
BB Apr 26, 2013 BB May 24, 2013
Where it was sold
California New Jersey
FDA's distribution note: California, New Jersey
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
- Golden Dharma International Corp
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 18, 2013
- In FDA report of
- Mar 20, 2013
- Terminated
- Mar 12, 2013
- FDA recall number
- F-1131-2013 · event 34821
- Official record
- FDA enforcement report search