Snack Innovations Inc. Recall: May contain undeclared peanut residue.

🇺🇸 United States

1. January 20, 2023 - Recall initiated
2. March 8, 2023 - Reported by source
3. August 9, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0395-2023

Event ID

91558

Status

Terminated

Classification

Class III

Company

Snack Innovations Inc.

Product description

Drizzilicious Mini Rice Cake bites Net Wt. 4oz and/or .74oz Bags Salted Caramel UPC:857900005167 and 857900005181 Packaged in a plastic bags Product also packed in the Drizzilicious mini rice cakes 32-ct Variety box

Quantity

3224 cases

Reason

May contain undeclared peanut residue.

Recall initiation date

January 20, 2023

Report date

March 8, 2023

Classification date

Not published in this source record

Termination date

August 9, 2023

Distribution pattern

Distributed to distributors in OH, CT, CA, TX, MA, FL, NY, CO, RI, WA in the US.

UPC, lot, and code information

UPC 857900005167; Best By 08OCT2023 N3-11BHNV0083 Best By 22SEP2023 N4-11BHNV3562 Best By 19SEP2023 N4-21BHNV3532

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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 91558 with 7 other product entries in Public Health Trace.

Responsible company: Snack Innovations Inc.

Other recalls from Snack Innovations Inc.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Ohio	1
Connecticut	1
California	1
Texas	1
Massachusetts	1
Florida	1
New York	1
Colorado	1
Rhode Island	1
Washington	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.

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