Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit
Summary
The FDA issued a Class II for Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit by Tony's Tejas Salsa. Reason: Production Process not approved for acidified foods..
Details
Source
Food Recall
External ID
F-0878-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit
Lot/Code Info: 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
Quantity Affected: 80 units
Reason for Recall
Production Process not approved for acidified foods.
Distribution
Alabama, Louisiana, Mississippi, and Tennessee
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-28
Company
Mobile, AL
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 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tony's Tejas Salsa has 5 FDA actions in our database, including 5 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 (Tony's Tejas Salsa) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tony's Tejas Salsa have FDA actions?
Tony's Tejas Salsa has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0878-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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