Kinder Mix Chocolate Treats Basket 5.3 OZ (152g) cardboard basket. UPC: 09800 60209. Best By: July 30, 2022
Summary
The FDA issued a Class II for Kinder Mix Chocolate Treats Basket 5.3 OZ (152g) cardboard basket. UPC: 09800 60 by FERRERO USA INC. Reason: Possible contamination with Salmonella Typhimurium..
Details
Source
Food Recall
External ID
F-1028-2022
Action Date
2022-05-04
Status
Terminated
Category
food
Product Description
Kinder Mix Chocolate Treats Basket 5.3 OZ (152g) cardboard basket. UPC: 09800 60209. Best By: July 30, 2022
Lot/Code Info: 03L 018AR - 306
Quantity Affected: 396 units
Reason for Recall
Possible contamination with Salmonella Typhimurium.
Distribution
Distributed to retail stores in CT, MA, RI, MI, PA, NY, FL, NH, SC, MD, ME, NJ, VA, DE, GA, NC, OH, CA, and NV
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-07
Company
Parsippany, NJ
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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
FERRERO USA INC has 2 FDA actions in our database, including 2 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 (FERRERO USA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FERRERO USA INC have FDA actions?
FERRERO USA INC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1028-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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