RecallHawk
Class II Recall

Aurora Natural brand; Organic Cranberry Frontier Mix UPC: 6 55852 00730 3; 19 oz (538g); Ingredients: ORGANIC DRIED CRAN

Aurora Products, Inc.

Summary

The FDA issued a Class II for Aurora Natural brand; Organic Cranberry Frontier Mix UPC: 6 55852 00730 3; 19 oz by Aurora Products, Inc.. Reason: Product contains undeclared peanuts..

Details

Source

Food Recall

External ID

F-0003-2023

Action Date

2022-10-12

Status

Terminated

Category

food

Product Description

Aurora Natural brand; Organic Cranberry Frontier Mix UPC: 6 55852 00730 3; 19 oz (538g); Ingredients: ORGANIC DRIED CRANBERRIES (ORGANIC CANE SUGAR, ORGANIC SUNFLOWER OIL), ORGANIC RAISINS, ORGANIC DATES (ORGANIC OAT COVERING), ORGANIC CASHEWS, ORGANIC PEPITAS, ORGANIC ALMONDS. CONTAINS: CASHEWS, ALMONDS. May Contain: Peanuts, Other Tree Nuts, Milk, Soy, Wheat, Sesame; DISTRIBUTED BY AURORA PRODUCTS, INC. ORANGE, CT 06477; BEST IF USED BY 05/16/23

Lot/Code Info: BEST IF USED BY 05/16/23 UPC: 6 55852 00730 3

Quantity Affected: 360 retail units

Reason for Recall

Product contains undeclared peanuts.

Distribution

ME, NH, MA, VT, NY

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-07

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 57 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 (Aurora Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Aurora Products, Inc. have FDA actions?

This is the only FDA action we have on record for Aurora Products, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0003-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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