RecallHawk
Class II Recall

Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376093 and Amla Alcohol-Free Extract, 4 oz. glass bottle, UPC 0

Secrets Of The Tribe

Summary

The FDA issued a Class II for Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376093 and Amla Alcohol by Secrets Of The Tribe. Reason: Product has elevated level of lead..

Details

Source

Food Recall

External ID

F-0072-2023

Action Date

2022-11-02

Status

Terminated

Category

food

Product Description

Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376093 and Amla Alcohol-Free Extract, 4 oz. glass bottle, UPC 041979376116, Secrets of the Tribe LLC, PO Box 5264, Denver, CO, 80217

Lot/Code Info: Batch ID: AMY6045 Best Before 01/11/2028

Quantity Affected: N/A

Reason for Recall

Product has elevated level of lead.

Distribution

Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-19

Company

Secrets Of The Tribe

Commerce City, CO

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

Secrets Of The Tribe has 2 FDA actions in our database, including 2 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 (Secrets Of The Tribe) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Secrets Of The Tribe have FDA actions?

Secrets Of The Tribe has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0072-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions