RecallHawk
Class II Recall

Hans Kissle Potato Salad White Homestyle, 10 lb. bulk case, UPC Codes: 00036217701003

Hans Kissle Company, LLC

Summary

The FDA issued a Class II for Hans Kissle Potato Salad White Homestyle, 10 lb. bulk case, UPC Codes: 000362177 by Hans Kissle Company, LLC. Reason: Undeclared egg and soy.

Details

Source

Food Recall

External ID

F-0503-2024

Action Date

2023-12-13

Status

Terminated

Category

food

Product Description

Hans Kissle Potato Salad White Homestyle, 10 lb. bulk case, UPC Codes: 00036217701003

Lot/Code Info: Use by Date 11/25/2023

Quantity Affected: 217 - 10 lb. cases

Reason for Recall

Undeclared egg and soy

Distribution

CT, MA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-09

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

Hans Kissle Company, LLC has 3 FDA actions in our database, including 3 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 (Hans Kissle Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Hans Kissle Company, LLC have FDA actions?

Hans Kissle Company, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0503-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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