a.) King Kullen brand Watermelon Halo; UPC: 85316-10392; 26 oz plastic container b.) Gracie's Kitchen brand Watermelon H
Summary
The FDA issued a Class II for a.) King Kullen brand Watermelon Halo; UPC: 85316-10392; 26 oz plastic container by Gracie's Kitchens Inc.. Reason: Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0344-2025
Action Date
2025-01-08
Status
Terminated
Category
food
Product Description
a.) King Kullen brand Watermelon Halo; UPC: 85316-10392; 26 oz plastic container b.) Gracie's Kitchen brand Watermelon Halo; UPC: 85316-10392; 26 oz plastic container
Lot/Code Info: a.) Sell By Dates: 11/11-11/21/24 b.) Sell By Dates: 11/11-11/21/24
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
New Haven, CT
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-0344-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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