PAISA Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED
Summary
The FDA issued a Class I for PAISA Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRI by Tama Corporation. Reason: Undeclared Allergens: Wheat, Soy, Yellow #5.
Details
Source
Food Recall
External ID
F-0297-2024
Action Date
2023-10-25
Status
Terminated
Category
food
Product Description
PAISA Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED
Lot/Code Info: Lot Numbers: 31082301, 07092301, 06092301, 05092301, 04092301, 29082301, 30082301, 28082301, 31072301, 01082301, 02082301, 03082301, 08082301, 09082301, 10082301, 14082301, 15082301, 16082301, 17082301, 21082301, 22082301, 23082301, 24072301, 25072301, 26072301, 31072301, 28082301, 21072301, 27072301, 17082301, 14082301, 20072301, 21072301, 26072301, 07082301, 08062301, 30082301, 24082301, 12072301. Exp. Date: From 09/15/2023 to 11/12/2023
Quantity Affected: 8,230 packages (units)
Reason for Recall
Undeclared Allergens: Wheat, Soy, Yellow #5
Distribution
Domestic distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-15
Company
Doral, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tama Corporation has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Tama Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tama Corporation have FDA actions?
Tama Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0297-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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