Ittella International, LLC Recall: A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredient and the allergen information statement disclosed the presence of EGGS, WHEAT, MILK, SOY, COCONUT, in bolded text.

🇺🇸 United States

1. January 4, 2021 - Recall initiated
2. April 20, 2022 - Reported by source
3. April 11, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0992-2022

Event ID

89927

Status

Terminated

Classification

Class II

Company

Ittella International, LLC

Product description

Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569 Packed for: Tattooed Chef Paramount, CA 90723

Quantity

12213 cases

Reason

A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredient and the allergen information statement disclosed the presence of EGGS, WHEAT, MILK, SOY, COCONUT, in bolded text.

Recall initiation date

January 4, 2021

Report date

April 20, 2022

Classification date

Not published in this source record

Termination date

April 11, 2022

Distribution pattern

Nationwide

UPC, lot, and code information

UPC 850015982569; Lot code Best by Date 20A-325 5/20/2022 20P-325 5/20/2022 20A-327 5/22/2022 20P-327 5/22/2022 20A-328 5/23/2022 20P-328 5/23/2022 20A-329 5/24/2022 20P-329 5/24/2022 20A-335 5/30/2022 20P-335 5/30/2022 20A-336 6/1/2022 20P-336 6/1/2022 20A-337 6/2/2022 20P-337 6/2/2022 20A-338 6/3/2022 20P-338 6/3/2022 20A-356 6/21/2022 20P-356 6/21/2022 20A-357 6/22/2022 20P-357 6/22/2022 20A-358 6/23/2022 20P-358 6/23/2022

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Other

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Ittella International, LLC

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.

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