two-bite vanilla cupcakes 10 oz. UPC 7 70981 03109 5 284 g UPC 7 70981 73109 4 Bakery Fresh Goodness mini vanilla cupca
Summary
The FDA issued a Class II for two-bite vanilla cupcakes 10 oz. UPC 7 70981 03109 5 284 g UPC 7 70981 73109 4 by GIVE AND GO. Reason: Potential for metal in product.
Details
Source
Food Recall
External ID
F-0296-2022
Action Date
2021-12-29
Status
Terminated
Category
food
Product Description
two-bite vanilla cupcakes 10 oz. UPC 7 70981 03109 5 284 g UPC 7 70981 73109 4 Bakery Fresh Goodness mini vanilla cupcakes 10 oz. UPC 0 11110 18230 2 NL Vanilla cupcakes 12PK - Everyday 03540 7.52 lbs. case UPC 1 07 70981 03540 3 7 Select vanilla mini cupcakes 10 oz. UPC 0 52548 62682 2 Best Choice Bakery vanilla two-bite cupcakes 10 oz. UPC 0 70038 66154 2 Sweet P's bake shop vanilla cupcakes 10 oz. 0 11225 12601 7 Freshness Guaranteed vanilla cupcakes 13.1 oz. UPC 0 78742 36760 6 Kimberley's bakeshoppe vanilla cupcakes 11.2 oz. UPC 7 70981 31008 4 meijer vanilla cupcakes 11.2 oz. UPC 7 08820 65030 5
Lot/Code Info: UPC 7 70981 03109 5 Lots 21286, 21287 UPC 7 70981 73109 4 Lots 21292 UPC 0 11110 18230 2 Lots 21281, 21285, 21286, 21299, 21300 case UPC 1 07 70981 03540 3 Lots 21298 UPC 0 52548 62682 2 Lots 21286 UPC 0 70038 66154 2 Lots 21286 UPC 0 11225 12601 7 Lots 21299 UPC 0 78742 36760 6 Lots 21281, 21297 UPC 7 70981 31008 4 Lots 21301, 21302 UPC 7 08820 65030 5 Lots 21298
Quantity Affected: 1,142,754 retail units (total)
Reason for Recall
Potential for metal in product
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-08
Company
Etobicoke, N/A
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.
GIVE AND GO has 31 FDA actions in our database, including 31 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 (GIVE AND GO) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GIVE AND GO have FDA actions?
GIVE AND GO has 31 FDA actions in our database, including 31 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0296-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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