FDA recall record
Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77469 1. The label is read in...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 11, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77469 1.
The label is read in parts: ***Dark Chocolate***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter, Apple/Plum, Dark Chocolate, Oats, Brown Rice Flour, Coconut, Palm Sugar, Coconut, Corn Starch, Tapioca Flour, Almonds, Sunflower seeds, Pecans, Flax Seeds, Egg Replacer, Sea Salt, Vanilla & Baking Soda***Contains almonds and coconut. May contain nut shell fragments***".
Reason
Product is recalled because the Ingredients statement declares Peanut, Almonds, Coconut, and Pecans but the Contains statement did NOT declare Peanut and Pecans. In addition, the label did not declare sulfites that came from Non-GMO apples.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77469 1.
The label is read in parts: ***Dark Chocolate***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter, Apple/Plum, Dark Chocolate, Oats, Brown Rice Flour, Coconut, Palm Sugar, Coconut, Corn Starch, Tapioca Flour, Almonds, Sunflower seeds, Pecans, Flax Seeds, Egg Replacer, Sea Salt, Vanilla & Baking Soda***Contains almonds and coconut. May contain nut shell fragments***".
Code information listed by FDA
All codes within expiry. Product distributed between 6/26/17 and 8/10/17.
Distribution and firm information
Recalling firm listed by FDA: Kelejete LLC
Firm location listed by FDA: Boise, ID, United States
Distribution reported by FDA: Distributed in CA, ID, FL, TN, and TX.
Product quantity listed by FDA: 457 bars
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.