Cesarina Cookies, Mini Linzer Tart, Apricot Raspberry, Net Weight 16oz (453.59g)
Summary
The FDA issued a Class II for Cesarina Cookies, Mini Linzer Tart, Apricot Raspberry, Net Weight 16oz (453.59g) by Cesarina Bakery, Inc. Reason: Undeclared Milk.
Details
Source
Food Recall
External ID
F-0342-2022
Action Date
2021-12-29
Status
Terminated
Category
food
Product Description
Cesarina Cookies, Mini Linzer Tart, Apricot Raspberry, Net Weight 16oz (453.59g)
Lot/Code Info: LOT 8518 EXP 4/4/2022, LOT 8536 EXP 4/15/2022, LOT 8541 EXP 4/16/2022, LOT 8545 EXP 4/17/2022, LOT 8548 EXP 4/18/2022, LOT 8575 EXP 5/3/2022
Quantity Affected: 214 cases/12 units ea.
Reason for Recall
Undeclared Milk
Distribution
Domestic distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-24
Company
Seminole, FL
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 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Cesarina Bakery, Inc has 12 FDA actions in our database, including 12 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 (Cesarina Bakery, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cesarina Bakery, Inc have FDA actions?
Cesarina Bakery, Inc has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0342-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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