RecallHawk
Class II Recall

Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.

Lidl US TRADING

Summary

The FDA issued a Class II for Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 by Lidl US TRADING. Reason: Undeclared Egg, Milk, Wheat.

Details

Source

Food Recall

External ID

F-1448-2023

Action Date

2023-08-23

Status

Terminated

Category

food

Product Description

Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.

Lot/Code Info: Expiration: 15.03.2024

Quantity Affected: 948-1,000 units

Reason for Recall

Undeclared Egg, Milk, Wheat

Distribution

Imported product directly shipped to a warehouse in Virginia and then distributed to 3 distribution centers in North Carolina, Virginia, and Maryland. From the distribution centers distributed to Lidl retail stores in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-14

Company

Lidl US TRADING

Arlington, VA

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

Lidl US TRADING has 15 FDA actions in our database, including 15 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 (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lidl US TRADING have FDA actions?

Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1448-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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