Carbquik Mug Cake Double Chocolate Chunk, Net Wt. 9 oz 1.5oz packaged in foil pouch 6 servings per pouch, 24 pouches
Summary
The FDA issued a Class I for Carbquik Mug Cake Double Chocolate Chunk, Net Wt. 9 oz 1.5oz packaged in foil by Tova Industries Inc. Reason: Undeclared Allergen- Milk.
Details
Source
Food Recall
External ID
F-0915-2022
Action Date
2022-04-06
Status
Terminated
Category
food
Product Description
Carbquik Mug Cake Double Chocolate Chunk, Net Wt. 9 oz 1.5oz packaged in foil pouch 6 servings per pouch, 24 pouches per case
Lot/Code Info: Lot 02212071B Product No. 14926 Best Buy 07/26/22
Quantity Affected: 1700 cases
Reason for Recall
Undeclared Allergen- Milk
Distribution
Amazon distribution center located in NM
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-03
Company
Louisville, KY
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 23 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tova Industries Inc has 3 FDA actions in our database, including 3 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 (Tova Industries Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tova Industries Inc have FDA actions?
Tova Industries Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0915-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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