RecallHawk
Class II Recall

Sweet Cheese Pierogi Grandma s Cuisine Sweet Cheese Pierogi 0 67355 00034 5 16oz (454g) / 1 dozen Bernat s Sweet Cheese

DYMSKI PIEROGI LLC

Summary

The FDA issued a Class II for Sweet Cheese Pierogi Grandma s Cuisine Sweet Cheese Pierogi 0 67355 00034 5 16o by DYMSKI PIEROGI LLC. Reason: Undeclared milk and wheat.

Details

Source

Food Recall

External ID

F-1097-2022

Action Date

2022-06-08

Status

Terminated

Category

food

Product Description

Sweet Cheese Pierogi Grandma s Cuisine Sweet Cheese Pierogi 0 67355 00034 5 16oz (454g) / 1 dozen Bernat s Sweet Cheese 16oz (450g) Golden Eagle Sweet Cheese Pierogis 14 oz

Lot/Code Info: all lots

Quantity Affected: 1,721 units

Reason for Recall

Undeclared milk and wheat

Distribution

Distributed to retail stores, restaurants, and distribution centers in NJ, MA, and PA.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-06

Company

DYMSKI PIEROGI LLC

E Stroudsburg, PA

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

DYMSKI PIEROGI LLC has 9 FDA actions in our database, including 9 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 (DYMSKI PIEROGI LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DYMSKI PIEROGI LLC have FDA actions?

DYMSKI PIEROGI LLC has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1097-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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