RecallHawk
Class II Recall

Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic container (UPC 6-281103 300011). Each case contains 48-125

Tomoorona LLC

Summary

The FDA issued a Class II for Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic container (UPC 6-2 by Tomoorona LLC. Reason: The product is labeled to contain sodium caseinate, a milk derivative, but the label does not declare the product contains "milk.".

Details

Source

Food Recall

External ID

F-0077-2023

Action Date

2022-11-02

Status

Terminated

Category

food

Product Description

Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic container (UPC 6-281103 300011). Each case contains 48-125g containers.

Lot/Code Info: P: 04/01/22

Quantity Affected: 4 boxes

Reason for Recall

The product is labeled to contain sodium caseinate, a milk derivative, but the label does not declare the product contains "milk."

Distribution

Distributed to retail stores in IN, GA, KS and PA and direct to consumers.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-09

Company

Tomoorona LLC

Maryland Heights, MO

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.

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

How often does Tomoorona LLC have FDA actions?

This is the only FDA action we have on record for Tomoorona LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0077-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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