two-bite red velvet cupcakes 10 oz. UPC 7 70981 05520 6 Marketside red velvet cupcakes 10 oz. UPC 6 81131 10150 9 11.7
Summary
The FDA issued a Class II for two-bite red velvet cupcakes 10 oz. UPC 7 70981 05520 6 Marketside red velvet c by GIVE AND GO. Reason: Potential for metal in product.
Details
Source
Food Recall
External ID
F-0299-2022
Action Date
2021-12-29
Status
Terminated
Category
food
Product Description
two-bite red velvet cupcakes 10 oz. UPC 7 70981 05520 6 Marketside red velvet cupcakes 10 oz. UPC 6 81131 10150 9 11.7 oz. UPC 6 81131 24843 3 NL two-bite Red Velvet Premium Cupcakes 12PK 05620 7.52 lbs. case UPC 1 07 70981 05620 0 Favorite Day Gourmet red velvet filled cupcakes 11.7 oz. UPC 0 85239 42016 4 Kimberley's bakeshoppe red velvet filled gourmet cupcakes 11.7 oz. UPC 7 70981 31005 3
Lot/Code Info: UPC 7 70981 05520 6 Lots 21285, 21286, 21297, 21298, 21299, 21300, 21301 UPC 6 81131 10150 9 Lots 21297, 21302 case UPC 1 07 70981 05620 0 Lots 21300, 212301 UPC 0 85239 42016 4 Lots 21298 UPC 7 70981 31005 3 Lots 21286, 21298 UPC 6 81131 24843 3 Lots 21299
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-0299-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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