FoodDec 28, 2016
Real Fudge Coconut Fudge, brand Real Fudge recall — FDA F-0761-2017
Coconut Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
Recall history in this database
Classification mix: Class II: 9.
FoodDec 28, 2016
Real Fudge Plain Fudge, brand Real Fudge recall — FDA F-0754-2017
Plain Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge White Fudge Oreo, brand Real Fudge recall — FDA F-0753-2017
White Fudge Oreo is recalled due to undeclared wheat and blue # 1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge White Fudge, brand Real Fudge recall — FDA F-0760-2017
White Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge Rocky Road Fudge, brand Real Fudge recall — FDA F-0757-2017
Rocky Road Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge Peanut Butter Fudge, brand Real Fudge recall — FDA F-0756-2017
Peanut Butter Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge Salted Caramel Fudge, brand Real Fudge recall — FDA F-0759-2017
Salted Caramel Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge Nutty fudge, brand Real Fudge recall — FDA F-0755-2017
Nutty fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
FoodDec 28, 2016
Real Fudge Dark Chocolate Fudge, brand Real Fudge recall — FDA F-0758-2017
Dark Chocolate Fudge is recalled due to undeclared blue #1.
Class IIFDA: TerminatedReal Fudge
Understanding this recall history
This page summarizes recall records in which the official source identifies Real Fudge as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.