14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola P2006 (9 Frozen Pancakes). Barcode:01069150301620069
Summary
The FDA issued a Class I for 14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola P2006 (9 Fro by Gourmet Kitchen, Inc.. Reason: Undeclared almonds.
Details
Source
Food Recall
External ID
F-0866-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola P2006 (9 Frozen Pancakes). Barcode:0106915030162006992202425990
Lot/Code Info: Lot # 22024
Quantity Affected: 59 boxes
Reason for Recall
Undeclared almonds
Distribution
Distributed to 4 distributors and 21 direct accounts in VA, NJ, MI, PA, DE, GA, NY, OH, FL, HI, AZ, and DC.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-23
Company
Neptune, NJ
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 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Gourmet Kitchen, Inc. has 2 FDA actions in our database, including 2 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 (Gourmet Kitchen, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gourmet Kitchen, Inc. have FDA actions?
Gourmet Kitchen, 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-0866-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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