RecallHawk
Class II Recall

Universal Bakery Organic Aussie Bites, 30 oz clamshell container

Best Express Foods, Inc.

Summary

The FDA issued a Class II for Universal Bakery Organic Aussie Bites, 30 oz clamshell container by Best Express Foods, Inc.. Reason: Product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten..

Details

Source

Food Recall

External ID

F-1419-2024

Action Date

2024-07-03

Status

Ongoing

Category

food

Product Description

Universal Bakery Organic Aussie Bites, 30 oz clamshell container

Lot/Code Info: BBD 06/16/2024 LOT # BEF2 059 02 24 BBD 08/01/2024 Lot# BEF2 113 04 24

Quantity Affected: 12,538 units

Reason for Recall

Product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.

Distribution

U.S. Distribution to WA and IL.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-17

Company

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

Best Express Foods, Inc. has 4 FDA actions in our database, including 4 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 (Best Express Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Best Express Foods, Inc. have FDA actions?

Best Express Foods, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1419-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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