RecallHawk
Class I Recall

NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps

OBC GROUP CORP

Summary

The FDA issued a Class I for NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie by OBC GROUP CORP. Reason: Product appears to be Yellow Oleander instead of Nuez de la India as labeled..

Details

Source

Food Recall

External ID

F-1544-2023

Action Date

2023-09-27

Status

Terminated

Category

food

Product Description

NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps

Lot/Code Info: Exp. Date 11/2025

Quantity Affected: Unknown

Reason for Recall

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-09-05

Company

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

OBC GROUP CORP has 2 FDA actions in our database, including 2 recalls.

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 (OBC GROUP CORP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does OBC GROUP CORP have FDA actions?

OBC GROUP CORP 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-1544-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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