RecallHawk
Class II Recall

Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Origin Vietnam

Spices USA Inc.

Summary

The FDA issued a Class II for Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Orig by Spices USA Inc.. Reason: Due to elevated levels of lead in ground cinnamon.

Details

Source

Food Recall

External ID

F-1122-2024

Action Date

2024-04-17

Status

Terminated

Category

food

Product Description

Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Origin Vietnam

Lot/Code Info: Lot No: VN/OFD/1D/0623

Quantity Affected: 394 bags/21713.34 Lbs

Reason for Recall

Due to elevated levels of lead in ground cinnamon

Distribution

Distributors in 3 states: FL, GA, and NC; Trinidad and Tobago (W.I.); Guayana

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-12

Company

Spices USA Inc.

Hialeah, FL

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 (Spices USA Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Spices USA Inc. have FDA actions?

This is the only FDA action we have on record for Spices USA Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1122-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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