Local Fixe LLC Recall: Flour is declared but Wheat is not declared on label.

🇺🇸 United States

1. December 17, 2021 - Recall initiated
2. January 19, 2022 - Reported by source
3. March 1, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0393-2022

Event ID

89271

Status

Terminated

Classification

Class II

Company

Local Fixe LLC

Product description

Squid Ink- Fettucine is raw fresh pasta portioned into 4 ounce portions. Each portion is rolled in a wax deli sheet and bulk packaged into a reusable plastic container with varying weight. Each container will have 40-60 portions, net wt. 10-15 lbs (4.536-6.804 kg). The label is read in parts: "***Squid Ink- Fettucine ***Ingredients: Flour, Semolina flour, egg, Squid ink***www.localfixe.com***".

Quantity

456 pounds

Reason

Flour is declared but Wheat is not declared on label.

Recall initiation date

December 17, 2021

Report date

January 19, 2022

Classification date

Not published in this source record

Termination date

March 1, 2022

Distribution pattern

Distributed in OR only.

UPC, lot, and code information

Lot code 44536 and smaller

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

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 89271 with 5 other product entries in Public Health Trace.

Responsible company: Local Fixe LLC

Other recalls from Local Fixe LLC

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
Oregon	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 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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