FRENCH S CRISPY FRIED ONIONS ORIG 240/26.5 OZ PDM
Summary
The FDA issued a Class II for FRENCH S CRISPY FRIED ONIONS ORIG 240/26.5 OZ PDM by McCormick & Company, Inc.- Consumer Product Division. Reason: Potential growth of Staphylococcus aureus.
Details
Source
Food Recall
External ID
F-1214-2024
Action Date
2024-05-08
Status
Terminated
Category
food
Product Description
FRENCH S CRISPY FRIED ONIONS ORIG 240/26.5 OZ PDM
Lot/Code Info: UPC: 041500959030, July 23, 2025
Quantity Affected: 26.5 ounce - 720 Pouches
Reason for Recall
Potential growth of Staphylococcus aureus
Distribution
The product was distributed to the following States: AZ, IL
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-18
Company
Hunt Valley, MD
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
McCormick & Company, Inc.- Consumer Product Division has 2 FDA actions in our database, including 2 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 (McCormick & Company, Inc.- Consumer Product Division) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does McCormick & Company, Inc.- Consumer Product Division have FDA actions?
McCormick & Company, Inc.- Consumer Product Division has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1214-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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