Food Recall Check
Class III · Low risk Terminated Initiated May 4, 2012 (14 years ago)

FunFresh Foods World Berry Organic Cacao Nibs recall

Recalled by FunFresh Foods Inc · Ogden, UT, United States

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

Why it was recalled

FunFresh Foods World Berry Cacao Nibs 6 oz snack food contaminated with E. coli.

Pathogen: E. coli

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

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

FunFresh Foods World Berry Organic Cacao Nibs 6 oz, packaged in blue, brown, red, white, black and green packaging with red, black, yellow, white, and green print writing. The packaging is resealable.

Quantity: 500 x 6 oz units

Where it was sold

Alaska Arkansas Arizona California Connecticut Florida Georgia Idaho Illinois Indiana Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota New Hampshire New Jersey New Mexico Ohio Oklahoma Oregon South Carolina Tennessee Texas Washington Wisconsin West Virginia

FDA's distribution note: Product was distributed to health and natural food retail stores located in the following states: AK, AR, AZ, CA, CT, FL, GA, ID, IL, IN, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, OH, OK, OR, SC, SC, TN, TX, WA, WI, and WV.

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
FunFresh Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 4, 2012
In FDA report of
Aug 22, 2012
Terminated
Aug 17, 2012
FDA recall number
F-1328-2012 · event 61795
Official record
FDA enforcement report search