Kelejete LLC FDA recall records

The FDA has published 3 food recall enforcement records naming Kelejete LLC between 2017 and 2017, covering 1 separate recall events. The firm is recorded in Idaho. Data last updated 2 September 2026.

Records of 29,386
3
Share of all recalls
0%
Class I of 3
3
Reported between
2017 to 2017

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 3 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

3 of these records are Class I, 0 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 3 records.
ReportedProductFirmReasonClass
2017-09-27Cranberry Raisin Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77471 4. The label is read in parts: ***Cranberry Raisin ***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter, Apple/Plum, Oats, Raisins, Cranberries, 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***".Kelejete LLCProduct 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.Class I
2017-09-27Dark 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***".Kelejete LLCProduct 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.Class I
2017-09-27Chocolate 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***".Kelejete LLCProduct 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.Class I

Questions

How many FDA recalls has Kelejete LLC had?
The FDA has published 3 food recall enforcement records naming Kelejete LLC between 2017 and 2017. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.