Food, drugs, devices › Whole Foods Market
Food recall: Jivara Lactee Milk Chocolate Valrhona; 40% Ingredients: Cocoa Butter, whole powdered milk, sugar, cocoa beans, brown sug
FDA enforcement event 71338 is a food recall by Whole Foods Market of Emeryville, CA, initiated 23 May 2015 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 46% of the 607 food enforcement events initiated in 2015 carry the same class.
Status: Terminated, terminated 22 Jun 2015. Initiation: voluntary: firm initiated. Whole Foods Market has 64 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Whole Foods Market, Emeryville, CA.
Reason for recall
"One retail location incorrectly labeled Jivara Lactee Milk Chocolate Valrhona cut and wrap pieces without hazelnuts declared on the product label."
Distribution
"CA"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2738-2015 | Jivara Lactee Milk Chocolate Valrhona; 40% Ingredients: Cocoa Butter, whole powdered milk, sugar, cocoa beans, brown sugar, natural vanilla extract, soya lecithin, malt extract, Natural Vanilla Flavor. Contains: Soy,. May contain trace amounts of dairy, eggs, nuts and gluten as it produced on the same machinery. UPC… | xx | Class II | Terminated | 1 Jul 2015 |
Context
Other enforcement events for Whole Foods Market
All 64 events for Whole Foods Market
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "One retail location incorrectly labeled Jivara Lactee Milk Chocolate Valrhona cut and wrap pieces without hazelnuts declared on the product label."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "CA"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 22 Jun 2015. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.