RecallHawk
Class II Recall

Steakhouse Potato Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest T

Morski Brands, Inc.

Summary

The FDA issued a Class II for Steakhouse Potato Salad, Keep Refrigerated packaged in the following brands and by Morski Brands, Inc.. Reason: Foreign object (metal)..

Details

Source

Food Recall

External ID

F-1373-2022

Action Date

2022-06-22

Status

Terminated

Category

food

Product Description

Steakhouse Potato Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest Traditions, Net Wt. 10 lb (4.54kg), Item 1038364. UPC 10-73314710773-4. Mfg By Morski Brands, Inc., Portage, WI 53801. 2. Finest Traditions, Net Wt. 6-16 oz (2.72kg), Item 1059716. UPC 7 33147 08357 4. Distributed By: DBC Foods, St. Cloud, MN 56302. 3. Dawn's Net Wt. 10 lb (4.54kg). Item # 10102. UPC 0 32345 10102 9. Mfg By Morski Brands, Inc., Portage, WI 53801.

Lot/Code Info: Best Before: 6-13-22 and 6-21-22

Quantity Affected: 2210 units

Reason for Recall

Foreign object (metal).

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-20

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

Morski Brands, Inc. has 6 FDA actions in our database, including 6 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 (Morski Brands, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Morski Brands, Inc. have FDA actions?

Morski Brands, Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1373-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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