RecallHawk
Class I Recall

SW Texas Nut Blend, Item #5180819, Packed in cardboard box with poly liner; net wt. 25 lbs. No UPC. Label declares: SW

Willamette Hazelnut, Inc.

Summary

The FDA issued a Class I for SW Texas Nut Blend, Item #5180819, Packed in cardboard box with poly liner; net by Willamette Hazelnut, Inc.. Reason: Undeclared Almonds and Cashews.

Details

Source

Food Recall

External ID

F-0893-2023

Action Date

2023-05-24

Status

Terminated

Category

food

Product Description

SW Texas Nut Blend, Item #5180819, Packed in cardboard box with poly liner; net wt. 25 lbs. No UPC. Label declares: SW Texas Nut Blend, ingredients: Hazelnuts, Walnuts. Manufactured by: Ardent Mills Ave. Tualatin, OR.

Lot/Code Info: Lot Code Production Date Expiration date 112595 3/17/2022 3/17/2023 112889 3/24/2022 3/24/2023 116839 8/31/2022 8/31/2023 116875 9/13/022 9/13/2023 115753 6/15/2022 6/15/2023 116486 7/22/2022 7/22/2023

Quantity Affected: 18,000 lbs.

Reason for Recall

Undeclared Almonds and Cashews

Distribution

Distributed in OR

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-13

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

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

How often does Willamette Hazelnut, Inc. have FDA actions?

Willamette Hazelnut, Inc. 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-0893-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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