Class II Recall

Squid Ink- Fettucine is raw fresh pasta portioned into 4 ounce portions. Each portion is rolled in a wax deli sheet and

Summary

The FDA issued a Class II for Squid Ink- Fettucine is raw fresh pasta portioned into 4 ounce portions. Each p by Local Fixe LLC. Reason: Flour is declared but Wheat is not declared on label..

Details

Source

Food Recall

External ID

F-0393-2022

Action Date

2022-01-19

Status

Terminated

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***".

Lot/Code Info: Lot code 44536 and smaller

Quantity Affected: 456 pounds

Reason for Recall

Flour is declared but Wheat is not declared on label.

Distribution

Distributed in OR only.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-12-17

Company

Local Fixe LLC

Roseburg, OR

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 146 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Local Fixe LLC has 6 FDA actions in our database, including 6 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Local Fixe LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Local Fixe LLC have FDA actions?

Local Fixe LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0393-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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