Carbquik Mug Cakes Cinnamon Spice, Net Wt. 9 oz 1.5oz mug cake mix packaged in foil pouch 6 servings per pouch, 24 p
Summary
The FDA issued a Class II for Carbquik Mug Cakes Cinnamon Spice, Net Wt. 9 oz 1.5oz mug cake mix packaged i by Tova Industries Inc. Reason: Undeclared Allergen- Milk.
Details
Source
Food Recall
External ID
F-0914-2022
Action Date
2022-04-06
Status
Terminated
Category
food
Product Description
Carbquik Mug Cakes Cinnamon Spice, Net Wt. 9 oz 1.5oz mug cake mix packaged in foil pouch 6 servings per pouch, 24 pouches per case
Lot/Code Info: Lot 01212071B Product No. 14927 Best By 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 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 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 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 (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-0914-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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