GIVE AND GO Recall: Potential for metal in product

🇺🇸 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-0299-2022

Event ID

89052

Status

Terminated

Classification

Class II

Company

GIVE AND GO

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

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 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

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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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.

• Email
• X / Twitter
• Facebook