RecallHawk
Class III Recall

Karlsburger Kitchens NSLP 140 Turkey Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32713. Net We

Karlsburger Foods, Inc.

Summary

The FDA issued a Class III for Karlsburger Kitchens NSLP 140 Turkey Gravy Mix, Gluten Free. Packaged in the fo by Karlsburger Foods, Inc.. Reason: undeclared non-wheat gluten, product labeled gluten-free.

Details

Source

Food Recall

External ID

F-0050-2023

Action Date

2022-10-26

Status

Terminated

Category

food

Product Description

Karlsburger Kitchens NSLP 140 Turkey Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32713. Net Weight 13 oz. (368 gm). 2. Item 32725. Net Weight 25 lb. (11.34 kg). Manufactured in a plant that handles Gluten. Karlsburger Foods, Inc., Monticello, MN 55362.

Lot/Code Info: 1091401, 2040701

Quantity Affected: 42 - 25 pound pails and 299 - 12 oz. pouches

Reason for Recall

undeclared non-wheat gluten, product labeled gluten-free

Distribution

KS, MN, NE, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-19

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Karlsburger Foods, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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

How often does Karlsburger Foods, Inc. have FDA actions?

Karlsburger Foods, 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-0050-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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