RecallHawk
Class I Recall

PAISA Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED

Tama Corporation

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

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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