Summary
The FDA issued a Class II for REGAL TACO SEASONING 10oz , 25#, 5# various containers. by Regal Foods, Inc. Reason: The firm initiated a recall of various seasonings because rodent feces was found in samples of oregano..
Details
Source
Food Recall
External ID
F-1609-2023
Action Date
2023-10-04
Status
Terminated
Category
food
Product Description
REGAL TACO SEASONING 10oz , 25#, 5# various containers.
Lot/Code Info: Code: REGAL TACO SEASONING 10oz ORE22183 REGAL TACO SEASONING 25# 8400 REGAL TACO SEASONING 5# ORE22183 REGAL TACO SEASONING 5# 8400
Quantity Affected: 1559 lbs.
Reason for Recall
The firm initiated a recall of various seasonings because rodent feces was found in samples of oregano.
Distribution
The product was distributed to the following states: GA, MD, PA, KY
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-20
Company
Leola, PA
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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Regal Foods, Inc has 8 FDA actions in our database, including 8 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 (Regal Foods, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Regal Foods, Inc have FDA actions?
Regal Foods, Inc has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1609-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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