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All American Seasonings, Inc. Recall: All American Seasonings is recalling Lost Cajun Gumbo Base because an ingredient was contaminated with Salmonella. - F-1008-2018

United States

TerminatedClass II

Company
All American Seasonings, Inc.
Product
LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended b…
Recall date
March 15, 2018
Terminated
June 27, 2018
Source
FDA

Reason for recall

All American Seasonings is recalling Lost Cajun Gumbo Base because an ingredient was contaminated with Salmonella.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended by ALL AMERICAN SEASONINGS, 10600 E. 54th Ave., Units B & C, Denver, CO 80239 Not published in this source record 23 bags Lot 80681, Manufacture Date: February 22, 2018

Distribution

  • One customer in Colorado.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1008-2018
Event ID
79539
Status
Terminated
Classification
Class II
Company
All American Seasonings, Inc.
Product description
LOST CAJUN GUMBO BASE, T4014, PACK SIZE 45 lb bag, Blended by ALL AMERICAN SEASONINGS, 10600 E. 54th Ave., Units B & C, Denver, CO 80239
Quantity
23 bags
Reason
All American Seasonings is recalling Lost Cajun Gumbo Base because an ingredient was contaminated with Salmonella.
Recall initiation date
March 15, 2018
Report date
April 18, 2018
Classification date
Not published in this source record
Termination date
June 27, 2018
Distribution pattern
One customer in Colorado.
UPC, lot, and code information
Lot 80681, Manufacture Date: February 22, 2018
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

Responsible company: All American Seasonings, Inc.

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Published
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Distribution
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Distribution
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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. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 27, 2018.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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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