Food recall: El Original pa' ya To Go by hot pandeyuca brand Soft Bread Pan Alinado
Hot Pandeyuca & Company Inc (Hialeah, FL) initiated this food recall on 21 Mar 2014; FDA lists 3 product records under event 68007, classified Class II.
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. 41% of the 573 food enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 25 Aug 2014. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Hot Pandeyuca & Company Inc.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Hot Pandeyuca & Company Inc, Hialeah, FL.
Reason for recall
"During an FDA inspection, it was discovered that the label of several products failed to declare the components ingredients of a butter flavor that included allergens FD&C Yellow #5, FD&C Yellow #6 and FD&C Red #40."
Distribution
"FL and NC Panama"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2015-2014 | El Original pa' ya To Go by hot pandeyuca brand Soft Bread Pan Alinado | 56 Boxes of 14 units each | Class II | Terminated | 18 Jun 2014 |
| F-2016-2014 | El Original pa' ya To Go by hot pandeyuca brand Cheese Bread Pan de Queso Grande | 1,052 boxes of 14 units each | Class II | Terminated | 18 Jun 2014 |
| F-2017-2014 | El Original pa' ya To Go by hot pandeyuca brand Small Cheese Bread Quesipan | 1,651 boxes of 50 units each | Class II | Terminated | 18 Jun 2014 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "During an FDA inspection, it was discovered that the label of several products failed to declare the components ingredients of a butter flavor that included allergens FD&C Yellow #5, FD&C Yellow #6 and FD&C Red #40."
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: "FL and NC Panama"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 25 Aug 2014. "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.