RecallHawk
Class II Recall

The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240

Spice House

Summary

The FDA issued a Class II for The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240 by Spice House. Reason: Undeclared sesame.

Details

Source

Food Recall

External ID

F-0281-2022

Action Date

2021-12-15

Status

Terminated

Category

food

Product Description

The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240

Lot/Code Info: No lot codes on product

Quantity Affected: 737 units

Reason for Recall

Undeclared sesame

Distribution

The product was only available for purchase from November 12 through November 18, 2021. The product is distributed nationally through online sales via www.thespicehouse.com and also is sold at the four The Spice House retail locations in Illinois and Wisconsin.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-18

Company

Spice House

Evanston, 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 60 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 (Spice House) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Spice House have FDA actions?

This is the only FDA action we have on record for Spice House in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0281-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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