Coborn's Inc, Carrot Cake Squares, 6 oz., Clam Shell Package, 12 per case
Summary
The FDA issued a Class I for Coborn's Inc, Carrot Cake Squares, 6 oz., Clam Shell Package, 12 per case by Royal Baking Corp.. Reason: The firm is recalling Coborn's Inc, Carrot Cake Squares, 6 oz., Clam Shell Package, 12 per case because of Undeclared Walnut Allergen ..
Details
Source
Food Recall
External ID
F-1299-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
Coborn's Inc, Carrot Cake Squares, 6 oz., Clam Shell Package, 12 per case
Lot/Code Info: SL21R 10222 12483 / SL21R 10322 12483 and SL21R 10822 12483
Quantity Affected: 144 cases
Reason for Recall
The firm is recalling Coborn's Inc, Carrot Cake Squares, 6 oz., Clam Shell Package, 12 per case because of Undeclared Walnut Allergen .
Distribution
Sold to customer in Greenville, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-17
Company
Moonachie, 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 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Royal Baking Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Royal Baking Corp. have FDA actions?
This is the only FDA action we have on record for Royal Baking Corp. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1299-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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