RecallHawk
Class II Recall

a.) King Kullen brand Diced White Onion; UPC: 85316-10083; 12 oz plastic container b.) Wild By Nature brand Diced White

Gracie's Kitchens Inc.

Summary

The FDA issued a Class II for a.) King Kullen brand Diced White Onion; UPC: 85316-10083; 12 oz plastic contain by Gracie's Kitchens Inc.. Reason: Product may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0329-2025

Action Date

2025-01-08

Status

Terminated

Category

food

Product Description

a.) King Kullen brand Diced White Onion; UPC: 85316-10083; 12 oz plastic container b.) Wild By Nature brand Diced White Onion; UPC: 85316-10085; 12 oz plastic container c.) Gracie's Kitchen brand Diced White Onion; UPC: 85316-10018; 10 oz plastic container d.) Gracie's Kitchen brand Diced White Onion; UPC: 85316-10085; 10 oz plastic container

Lot/Code Info: a.) Sell By Dates: 11/12-11/22/24 b.) Sell By Dates: 11/12-11/22/24 c.) Sell By Dates: 11/12-11/22/24 d.) Sell By Dates: 11/12-11/22/24

Quantity Affected: 3681 cases total

Reason for Recall

Product may be contaminated with Listeria monocytogenes.

Distribution

CT and NY

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-27

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

Gracie's Kitchens Inc. has 35 FDA actions in our database, including 35 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 (Gracie's Kitchens Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Gracie's Kitchens Inc. have FDA actions?

Gracie's Kitchens Inc. has 35 FDA actions in our database, including 35 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0329-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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