FDA recall record

THRIVE 6 Grain Pancake Mix recall — FDA F-1867-2013

Thrive Foods is recalling certain lots of its 64 and 72 ounce cans of THRIVE 6 Grain Pancake Mix because this product contains ingredients that react over…

Class IIIclassification
F-1867-2013official record ID
Sep 11, 2013report date

Recall record at a glance

Official recordF-1867-2013
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmThrive Foods LLC
Report dateSep 11, 2013
Recall initiation dateJul 25, 2013
QuantityGallon Cans - 100,116 cans; Pantry Cans - 4,219 cans
LocationAmerican Fork, UT, United States

Official product description

THRIVE 6 Grain Pancake Mix; There are two unit sizes: (1) 4 lb. #10/gallon can (6.03x 7.02) (the "Gallon Cans"); and (2) 1.17 lb. Pull-Top Pantry Cans (4.01x 5.08) (the "Pantry Cans"). Both units are packaged in metal cans. The Pantry Can has a metal pull-top lid and the Gallon Can has a metal lid that must be opened by a can opener. (1) The Gallon Cans may be ordered as single units or in six (6) can cases. (2) The Pantry Cans may be ordered as single units or in ten (10) can cases.

Why the product was recalled

Thrive Foods is recalling certain lots of its 64 and 72 ounce cans of THRIVE 6 Grain Pancake Mix because this product contains ingredients that react over time and increase the pressure inside the can, which may cause cans to expand or bulge and increase the risk of sudden release of the pancake mix when the can is opened and could pose the risk of injury.

Distribution information

The product was distributed nationwide, in all U.S. states, and in Canada (Wade & Sandy Pierson Company Name: In Case Of , #102 127 Commercial Drive , Calgary AB T3Z 2A7 Canada, Tel. 403-381-0005). The product was not distributed to the U.S. Defense Supply Center, VA or other Federal Government Agency Sales/distribution center.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

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