RecallHawk
Class II Recall

two-bite vanilla & chocolate cupcakes 10 oz. UPC 7 70981 03127 9 20 oz. UPC 7 70981 03104 0

GIVE AND GO

Summary

The FDA issued a Class II for two-bite vanilla & chocolate cupcakes 10 oz. UPC 7 70981 03127 9 20 oz. UPC 7 7 by GIVE AND GO. Reason: Potential for metal in product.

Details

Source

Food Recall

External ID

F-0287-2022

Action Date

2021-12-29

Status

Terminated

Category

food

Product Description

two-bite vanilla & chocolate cupcakes 10 oz. UPC 7 70981 03127 9 20 oz. UPC 7 70981 03104 0

Lot/Code Info: 10oz.: 21296 20oz.: 21291, 21292

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

GIVE AND GO

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-0287-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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