RecallHawk
Class II Recall

Wilbur¿ Dark Chocolate Covered Cashews Net Wt.16 oz (1 LB) 454g Packaged in plastic bag

Cargill Cocoa & Chocolate, Inc.

Summary

The FDA issued a Class II for Wilbur¿ Dark Chocolate Covered Cashews Net Wt.16 oz (1 LB) 454g Packaged in pla by Cargill Cocoa & Chocolate, Inc.. Reason: Undeclared peanut.

Details

Source

Food Recall

External ID

F-0770-2023

Action Date

2023-05-10

Status

Terminated

Category

food

Product Description

Wilbur¿ Dark Chocolate Covered Cashews Net Wt.16 oz (1 LB) 454g Packaged in plastic bag

Lot/Code Info: lot 230228HA

Quantity Affected: 17 bags

Reason for Recall

Undeclared peanut

Distribution

Distributed to 6 consumers in MN, NJ, OH, FL, RI, and KS

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-07

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

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

How often does Cargill Cocoa & Chocolate, Inc. have FDA actions?

Cargill Cocoa & Chocolate, 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-0770-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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