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Victoria Gourmet, Inc. Recall: Product contains undeclared sesame.

United States

TerminatedClass II

Company
Victoria Gourmet, Inc.
Product
Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement…
Recall date
November 17, 2020
Terminated
December 14, 2020
Source
FDA

Reason for recall

Product contains undeclared sesame.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in a glass jar. Canadian product only. Not published in this source record 1,080 jars 1-322756 Distributor Numbers: 137721; 016074

Distribution

  • Canada only.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0162-2021
Event ID
86865
Status
Terminated
Classification
Class II
Company
Victoria Gourmet, Inc.
Product description
Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in a glass jar. Canadian product only.
Quantity
1,080 jars
Reason
Product contains undeclared sesame.
Recall initiation date
November 17, 2020
Report date
December 16, 2020
Classification date
Not published in this source record
Termination date
December 14, 2020
Distribution pattern
Canada only.
UPC, lot, and code information
1-322756 Distributor Numbers: 137721; 016074
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

Responsible company: Victoria Gourmet, Inc.

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FDA Recall United States TerminatedTerminated: October 24, 2018Historical recordClass III

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Product
Victoria Taylor's Seasonings - New Orleans - 5.0 oz. UPC: 66…
Published
October 31, 2018
Distribution
Multiple states

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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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:

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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