Reduced Sodium Roast Beef Rub (Serv-Rite) NET WT: 50 lb UPC (QST# 6313)
Summary
The FDA issued a Class II for Reduced Sodium Roast Beef Rub (Serv-Rite) NET WT: 50 lb UPC (QST# 6313) by QST Ingredients and Packaging. Reason: Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing..
Details
Source
Food Recall
External ID
H-0495-2025
Action Date
2025-08-20
Status
Terminated
Category
food
Product Description
Reduced Sodium Roast Beef Rub (Serv-Rite) NET WT: 50 lb UPC (QST# 6313)
Lot/Code Info: Lot numbers: 092251, 112251, 133251, 160251, 181251
Quantity Affected: 7,950 pounds total
Reason for Recall
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Distribution
Product was distributed to 4 different customers who either use recalled finished product for ingredient in further processing or repack for retail sales. 4 customers are located in Southern California with the remaining customer in Texas.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-07
Company
Rancho Cucamonga, 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 113 food recalls issued in the same week, part of 204 food-related FDA actions this month.
QST Ingredients and Packaging has 4 FDA actions in our database, including 4 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 (QST Ingredients and Packaging) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does QST Ingredients and Packaging have FDA actions?
QST Ingredients and Packaging has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0495-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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