King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin package with a clear dome top marked wit
Summary
The FDA issued a Class I for King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin by Gracie's Kitchens Inc.. Reason: Product contains undeclared wheat and sesame..
Details
Source
Food Recall
External ID
F-1238-2024
Action Date
2024-05-08
Status
Terminated
Category
food
Product Description
King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin package with a clear dome top marked with a UPC Code 0 8531610145 0
Lot/Code Info: Sell By dates of: 4/14/24 - 4/21/24
Quantity Affected: 32 pieces
Reason for Recall
Product contains undeclared wheat and sesame.
Distribution
New York
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-09
Company
New Haven, CT
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 17 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 I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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-1238-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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