Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package…
Recalling firm: Kelejete LLC
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 11, 2017.
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616320774677FDA code information
All codes within expiry. Product distributed between 6/26/17 and 8/10/17.
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Full FDA record and distribution details
Original product description
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 77467 7. The label is read in parts: ***Chocolate***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter, Apple/Plum, Semisweet Chocolate, Oats, Brown Rice Flour, Coconut Palm Sugar, Coconut, Corn Starch, Tapioca Flour, Almonds, Sunflower Seeds, Pecans, Flas Seeds, Egg Replacer, Sea Salt, Vanilla & Baking Soda***Contains almonds and coconut. May contain nut shell fragments***".
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 616320774677 | a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77467 7. The label is read in parts: ***Chocolate***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter |
Original FDA recall 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.
Recall details
- Recall number
- F-3556-2017
- Event ID
- 77932
- FDA status
- Terminated
- Initiated
- Aug 13, 2017
- Reported
- Sep 27, 2017
- Classified
- Sep 21, 2017
- Terminated
- Oct 11, 2017
- Quantity
- 136 bars
- Location
- Boise, ID, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Distributed in CA, ID, FL, TN, and TX.
Data updated September 16, 2026. View official FDA data ↗
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