Summary
The FDA issued a Class II for TETAS Mireya, SABOR Nutella by DIBE LLC. Reason: Undeclared allergens: Soy.
Details
Source
Food Recall
External ID
F-0981-2023
Action Date
2023-06-14
Status
Terminated
Category
food
Product Description
TETAS Mireya, SABOR Nutella
Lot/Code Info: Exp. Date 10/31/23
Quantity Affected: 250 units
Reason for Recall
Undeclared allergens: Soy
Distribution
Domestic distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-10
Company
Miami, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DIBE LLC has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (DIBE LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DIBE LLC have FDA actions?
DIBE LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0981-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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