GIVE AND GO Recall: Potential for metal in product - F-0296-2022

🇺🇸 United States

1. November 8, 2021 - Recall initiated
2. December 29, 2021 - Reported by source
3. August 9, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0296-2022

Event ID

89052

Status

Terminated

Classification

Class II

Company

GIVE AND GO

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

Quantity

1,142,754 retail units (total)

Reason

Potential for metal in product

Recall initiation date

November 8, 2021

Report date

December 29, 2021

Classification date

Not published in this source record

Termination date

August 9, 2024

Distribution pattern

Nationwide

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 89052 with 10 other product entries in Public Health Trace.

Responsible company: GIVE AND GO

Other recalls from GIVE AND GO

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of August 9, 2024.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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