Recall Register

Food, drugs, devices

Food recall: TETAS Mireya, SABOR Galleta Maria

FDA enforcement event 92331 · Class I · initiated 10 Apr 2023 · status Terminated · terminated 29 Sep 2023

FoodVoluntary: Firm initiated5 product recordsMiami, FL

FDA enforcement event 92331 is a food recall by DIBE LLC of Miami, FL, initiated 10 Apr 2023 and classified Class I, with 5 product records.

FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 35% of the 478 food enforcement events initiated in 2023 carry the same class.

Status: Terminated, terminated 29 Sep 2023. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for DIBE LLC.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

DIBE LLC, Miami, FL.

Reason for recall

"Undeclared allergens: Soy"

Distribution

"Domestic distribution only."

Product records

Recall numberProductQuantityClassStatusReport date
F-0979-2023TETAS Mireya, SABOR Galleta Maria250 units/6oz ea.Class ITerminated14 Jun 2023
F-0980-2023TETAS Mireya, SABOR Ferrero250 units/6 oz ea.Class ITerminated14 Jun 2023
F-0981-2023TETAS Mireya, SABOR Nutella250 unitsClass IITerminated14 Jun 2023
F-0982-2023TETAS Mireya, SABOR Toddy250 units/6 oz ea.Class IITerminated14 Jun 2023
F-0983-2023TETAS Mireya, SABOR Galleta Oreo250 units/6 oz ea.Class ITerminated14 Jun 2023

Context

35%of 2023 food events are Class I478 events that year
5product records in this event
1event on this register for the firm

Questions and answers

Why was this food recalled?

FDA's record gives the reason for recall as: "Undeclared allergens: Soy"

What does Class I mean?

FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

Where was the product distributed?

FDA's distribution pattern field reads: "Domestic distribution only."

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 29 Sep 2023. "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.