FDA Recall United States Terminated Historical recordClass I
All American Seasonings, Inc.
- Product
- Super Nacho (No-Pho, Gluten Free). Product Code: T4034. 50 l…
- Published
- January 18, 2017
- Distribution
- Nationwide
All American Seasonings, Inc. Recall: All American Seasonings is recalling Lost Cajun Gumbo Base because an ingredient was contaminated with Salmonella.
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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
- 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.
Other recalls from All American Seasonings, Inc.
FDA Recall United States Terminated Historical recordClass I
All American Seasonings, Inc.
- Product
- Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags
- Published
- January 18, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
All American Seasonings, Inc.
- Product
- Triple Cheese Blend - No Color. Product Code: T4008. 50 lb b…
- Published
- January 18, 2017
- Distribution
- Nationwide
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:
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.
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