Cajun Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS units
Summary
The FDA issued a Class II for Cajun Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS units by Tampico Spice Company Inc. Reason: Product was found to have an elevated amount of Aflatoxin.
Details
Source
Food Recall
External ID
F-0404-2023
Action Date
2023-03-01
Status
Terminated
Category
food
Product Description
Cajun Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS units
Lot/Code Info: LOT# 2122483 & LOT# 301029
Quantity Affected: 5553 lbs (total)
Reason for Recall
Product was found to have an elevated amount of Aflatoxin
Distribution
CA, WA, AZ, OR, UT, TX, NV, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-02
Company
Los Angeles, CA
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 37 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tampico Spice Company Inc has 3 FDA actions in our database, including 3 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 (Tampico Spice Company Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tampico Spice Company Inc have FDA actions?
Tampico Spice Company Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0404-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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