Mountain View Bakery Chocolate Cake Roll 4oz or 8oz packaged in plastic clamshell sold individually
Summary
The FDA issued a Class II for Mountain View Bakery Chocolate Cake Roll 4oz or 8oz packaged in plastic clamshe by Mountain View Bakery. Reason: Undeclared Allergen - Milk.
Details
Source
Food Recall
External ID
F-0120-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Mountain View Bakery Chocolate Cake Roll 4oz or 8oz packaged in plastic clamshell sold individually
Lot/Code Info: Batch Numbers: 09/29/21 through 10/19/21 Best By Dates: 10/04/21 through 10/26/21
Quantity Affected: 19 units
Reason for Recall
Undeclared Allergen - Milk
Distribution
Distributed to Pilot gas stations within TN
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-19
Company
Chuckey, TN
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 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mountain View Bakery 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 (Mountain View Bakery) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mountain View Bakery have FDA actions?
Mountain View Bakery 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-0120-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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