Recall record at a glance
| Official record | F-1652-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Savory Foods, Inc. |
| Report date | Mar 19, 2014 |
| Recall initiation date | Jan 27, 2014 |
| Quantity | ~3424 all varieties |
| Location | Grand Rapids, MI, United States |
Official product description
MARY ANN'S Chocolates Signature Assortment,May Contain Sugar, Chocolate, Butter, Corn Syrup, Assorted Fruit and Nuts, Coconut, Vegetable Oil, Egg or Vegetable Albumen , Salt, Natural and Artificial Flavors and Certified Food Colors. Fruits Contain Sulfur Dioxide, Savory Foods, Inc. Grand Rapids, MI 49507 SIGNATURE ASSORTMENT 5PC, 3 oz UPC 733549030336 SIGNATURE ASSORTMENT 12PC-7OZ PINK BOX UPC 733549030343 CANDY-8OZ HEART BOXED ASSORTED CHOCOLATES 14.0 0Z BOX M CHOCOLATES SIGNATURE ASSORTMENT 13.0 OZ BOX M CHOCOLATES GRAND TRUFFLE ASSORTMENT 14 oz asstd UPC 733549030350 19 oz asstd UPC 733549030367 25 oz asstd UPC 733549030442 CANDY-CANDY-CANDY-GRAND TRUFFLE ASSTD 4 PC CANDY-GRAND TRUFFLE ASSTD 9 PC CANDY-ASSORTED SNAPPERS 5PC-5OZ PINK BOX Pictured Label placard on all boxes, all varieties: Mary Ann's Chocolates Signature Assortment: Lemon Creme Milk; Cherry Cordial Milk Raspberry Cream Milk, Tiramisu Truffle Dark, Caramel Milk/Dark Raspberry Truffle Dark, Almond Cluster Milk/Dark Chocolate; Coconut Cluster Milk, Chocolate Insanity Truffle Dark, Peanut Cluster Milk, Coconut Creme Milk, Maple Cream Milk, Pecan Cluster Milk, Irish Creme Truffle Dark
Why the product was recalled
The ingredient panel for assorted chocolates did not identify peanuts and specific tree nuts (almond, walnut, pecan, pistachio, cashew, macadamia and coconut). The source of lecithin was not identified as soy and lakes yellow 5, lakes yellow 6, red 3, red 40 and blue lake 1 were not identified as ingredients.
Distribution information
Michigan, Vermont, California, Georgia
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
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About this record
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