RecallHawk
Class II Recall

Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886

Eastland Food Corporation

Summary

The FDA issued a Class II for Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886 by Eastland Food Corporation. Reason: Cashews declared in ingredients statement but not in the contains statement..

Details

Source

Food Recall

External ID

F-0690-2023

Action Date

2023-04-12

Status

Terminated

Category

food

Product Description

Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886

Lot/Code Info: All lots

Quantity Affected: 5,235 cases

Reason for Recall

Cashews declared in ingredients statement but not in the contains statement.

Distribution

Distributed in FL, IA, IN, KS, MI, MN, MO, NE, OH, WI, CT, KY, MA, MD, ME, NC, NH, NJ, NY, PA, VA, WV, AL, GA, LA, MS, SC, TN and TX.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-01-14

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

Eastland Food Corporation has 7 FDA actions in our database, including 7 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 (Eastland Food Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Eastland Food Corporation have FDA actions?

Eastland Food Corporation has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0690-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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