RecallHawk
Class I Recall

Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and Niwal

GLOBAL MIX INC.

Summary

The FDA issued a Class I for Tejocote Root Products under the following brands: Eva Nutrition, Science of Alp by GLOBAL MIX INC.. Reason: Product contains Yellow Oleander.

Details

Source

Food Recall

External ID

F-1390-2024

Action Date

2024-07-03

Status

Terminated

Category

food

Product Description

Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and Niwali Mexican

Lot/Code Info: Serial No 181121U MFG Date: 8/1/2023 Expiry Date: 06/2025

Reason for Recall

Product contains Yellow Oleander

Distribution

Alabama, Alaska, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, New Carolina, New York, New Jersey, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming

Type: Voluntary: Firm initiated

Recall Initiated: 2024-04-05

Company

GLOBAL MIX INC.

Maspeth, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (GLOBAL MIX INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does GLOBAL MIX INC. have FDA actions?

This is the only FDA action we have on record for GLOBAL MIX INC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1390-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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