RecallHawk
Class II Recall

SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case

RAJA FOODS LLC

Summary

The FDA issued a Class II for SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 by RAJA FOODS LLC. Reason: Product tested positive for lead.

Details

Source

Food Recall

External ID

F-1126-2024

Action Date

2024-04-17

Status

Terminated

Category

food

Product Description

SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case

Lot/Code Info: Batch KX21223 Best Before July 2026

Quantity Affected: 200 cases (for all products)

Reason for Recall

Product tested positive for lead

Distribution

NY, NJ, PA, MD, VA, CT, MA, NH, TN, FL, GA, AL, NC, IL MS

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-07

Company

RAJA FOODS LLC

Skokie, IL

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

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 (RAJA FOODS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does RAJA FOODS LLC have FDA actions?

This is the only FDA action we have on record for RAJA FOODS LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1126-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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