RecallHawk
Class II Recall

Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g SKU# 51934-89685 UPC 0051 9342 Contains

Andersen & Sons Shelling, Inc.

Summary

The FDA issued a Class II for Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g by Andersen & Sons Shelling, Inc.. Reason: Product mispackaging; mixed nuts (cashews, macadamia, and walnuts) packed into bags labeled walnut pieces..

Details

Source

Food Recall

External ID

F-0983-2021

Action Date

2021-09-22

Status

Terminated

Category

food

Product Description

Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g SKU# 51934-89685 UPC 0051 9342 Contains Walnuts Dist & Sold Exclusive By: Trader Joe's, Monrovia, CA 91016

Lot/Code Info: Lot code 10299 Expiration Date 4/20/2022

Quantity Affected: 12,288 units

Reason for Recall

Product mispackaging; mixed nuts (cashews, macadamia, and walnuts) packed into bags labeled walnut pieces.

Distribution

U.S. distribution to the following: CT, NH. NY. RI, VT, ME, and MA. No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-01

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

Andersen & Sons Shelling, Inc. has 2 FDA actions in our database, including 2 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 (Andersen & Sons Shelling, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Andersen & Sons Shelling, Inc. have FDA actions?

Andersen & Sons Shelling, 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-0983-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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