Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram.
Kelejete LLC recalled this product and the FDA reported the enforcement action on 27 September 2017 as Class I. The recall was initiated by the firm. 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.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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***".
- UPC
- 616320774677
- Reason for recall
- 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.
- Recalling firm
- Kelejete LLC
- Firm location
- Boise, Idaho, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-3556-2017
- Quantity
- 136 bars
- Distribution
- Distributed in CA, ID, FL, TN, and TX.
- Initiated
- 13 August 2017
- Reported by FDA
- 27 September 2017
- Terminated
- 11 October 2017
- Firm notified by
- Product codes
- All codes within expiry. Product distributed between 6/26/17 and 8/10/17.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 3 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 3 of them.
- The recall ran for 8 weeks, from 13 August 2017 to termination on 11 October 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 4 states, and the FDA published the enforcement report 6 weeks after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was shorter than usual for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Idaho, Florida, Tennessee, Texas. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: peanuts, tree nuts, sulfites.
Filed under milk and dairy, fresh produce, nuts and seeds, snacks and confectionery, spices and seasonings, grains, flour and pasta, beverages and juice and eggs. A product can sit in more than one.
Other milk and dairy recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Kelejete LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 3 records for Kelejete LLC
All 2017 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. 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 accessRecall 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.