RecallHawk
Class II Recall

CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC venzutrade

VENZU TRADERS LLC

Summary

The FDA issued a Class II for CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Dist by VENZU TRADERS LLC. Reason: Potential contamination with heavy metal (lead)..

Details

Source

Food Recall

External ID

H-0466-2026

Action Date

2026-02-11

Status

Ongoing

Category

food

Product Description

CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC venzutraders@outlook.com

Lot/Code Info: UPC: 7 46241 29537 8

Quantity Affected: 24 cases (20 - 100g packs/case)

Reason for Recall

Potential contamination with heavy metal (lead).

Distribution

U.S. Distribution: CA, NV, WA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-14

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

How often does VENZU TRADERS LLC have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0466-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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