RecallHawk
Class II Recall

El Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , BOPP Bag, 12 units per cases

EL Chilar-HF, LLC

Summary

The FDA issued a Class II for El Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , BOPP Bag, 12 by EL Chilar-HF, LLC. Reason: Due to elevated levels of lead..

Details

Source

Food Recall

External ID

F-1092-2024

Action Date

2024-03-27

Status

Terminated

Category

food

Product Description

El Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , BOPP Bag, 12 units per cases

Lot/Code Info: Product Code #: 307 Lot # : D300 EXP 10/24 Lot #F272 EX 10/26

Quantity Affected: Lot code F272 EX1026: 127 Cases of 12 x 1.25 oz bags (165 lbs) and Lot code D300 EX1024: 127 Cases of 12 x 1.25 oz bags (165 lbs)

Reason for Recall

Due to elevated levels of lead.

Distribution

Product sent to distributors in MD

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.

EL Chilar-HF, LLC has 6 FDA actions in our database, including 6 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 (EL Chilar-HF, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does EL Chilar-HF, LLC have FDA actions?

EL Chilar-HF, LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1092-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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