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Tony's Tejas Salsa Recall: Production Process not approved for acidified foods.

United States

TerminatedClass II

Company
Tony's Tejas Salsa
Product
Port City Soups Thai Green Curry 32oz glass mason jar sol…
Recall date
February 28, 2022
Terminated
June 14, 2022
Source
FDA

Reason for recall

Production Process not approved for acidified foods.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit Not published in this source record 80 units Batch No: 221301, 222301, 220302, 220402, 222504, 2211901, 221602, 222001, 221102, 212912, 220701, 222401 Best By Dates: 12/29/22, 01/07/23, 01/13/23, 01/19/23, 01/20/23, 01/22/23, 01/23/23, 01/24/23, 01/25/23, 01/26/23, 02/03/23, 02/04/23, 02/16/23

Distribution

  • Alabama
  • Louisiana
  • Mississippi
  • and Tennessee

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0878-2022
Event ID
89724
Status
Terminated
Classification
Class II
Company
Tony's Tejas Salsa
Product description
Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit
Quantity
80 units
Reason
Production Process not approved for acidified foods.
Recall initiation date
February 28, 2022
Report date
March 23, 2022
Classification date
Not published in this source record
Termination date
June 14, 2022
Distribution pattern
Alabama, Louisiana, Mississippi, and Tennessee
UPC, lot, and code information
Batch No: 221301, 222301, 220302, 220402, 222504, 2211901, 221602, 222001, 221102, 212912, 220701, 222401 Best By Dates: 12/29/22, 01/07/23, 01/13/23, 01/19/23, 01/20/23, 01/22/23, 01/23/23, 01/24/23, 01/25/23, 01/26/23, 02/03/23, 02/04/23, 02/16/23
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

Other products recalled under this same event

This recall shares FDA event ID 89724 with 4 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Baton Rouge Beans 32oz glass mason jar so…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

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FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Alkaline Vegetable Soup 32oz glass mason j…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

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FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Tex-Mex Chili 32oz glass mason jar sold b…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

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FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Creole Gumbo 32oz glass mason jar sold by…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

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Responsible company: Tony's Tejas Salsa

Other recalls from Tony's Tejas Salsa

FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Baton Rouge Beans 32oz glass mason jar so…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

View recall →

FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Alkaline Vegetable Soup 32oz glass mason j…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

View recall →

FDA Recall United States Terminated Historical recordClass II

Tony's Tejas Salsa

Product
Port City Soups Tex-Mex Chili 32oz glass mason jar sold b…
Published
March 23, 2022
Distribution
Alabama, Louisiana, Mississippi, and Ten…

View recall →

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.

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.