RecallHawk
Class II Recall

La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449, packed in cello bags

la fiesta food products

Summary

The FDA issued a Class II for La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449, pa by la fiesta food products. Reason: Elevated levels of lead found in product.

Details

Source

Food Recall

External ID

F-1093-2024

Action Date

2024-03-27

Status

Terminated

Category

food

Product Description

La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449, packed in cello bags

Lot/Code Info: Lot code 25033

Quantity Affected: 16,044 individual bags (1337 dozens)

Reason for Recall

Elevated levels of lead found in product

Distribution

U.S. distribution to 319 retailers in California, Arizona, Washington and Texas.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-04

Company

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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.

la fiesta food products has 4 FDA actions in our database, including 4 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 (la fiesta food products) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does la fiesta food products have FDA actions?

la fiesta food products has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1093-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions