Summary
The FDA issued a Class II for Country Oven Boston Cream Cake Double Layer Cake 28oz by The Kroger Co. Reason: Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes..
Details
Source
Food Recall
External ID
F-0152-2022
Action Date
2021-11-17
Status
Terminated
Category
food
Product Description
Country Oven Boston Cream Cake Double Layer Cake 28oz
Lot/Code Info: UPC 0001111019561 Use By 04/04/22
Quantity Affected: 6 cases
Reason for Recall
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Distribution
Product distributed to the following states: SC, GA, AL, IL, IN, MO, OH, KY, WV, TN, MS, AR, NE, KS, CA, OR, AK, WA, ID, CO, LA, MT, NM, NV, TX, WI, WY, VA, UT
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-13
Company
Cincinnati, OH
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 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Kroger Co has 29 FDA actions in our database, including 29 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 (The Kroger Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Kroger Co have FDA actions?
The Kroger Co has 29 FDA actions in our database, including 29 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0152-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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