Duke's SOUTHERN SAUCES BAYOU REMOULADE NET WT. 10 FL OZ (296 ml) GLUTEN FREE INGREDIENTS:***SOY SAUCE (WHEAT, SOYBEANS,
Summary
The FDA issued a Class III for Duke's SOUTHERN SAUCES BAYOU REMOULADE NET WT. 10 FL OZ (296 ml) GLUTEN FREE ING by Sauer Brands, Inc.. Reason: The firm was notified by a consumer that the product label is incorrect. The label says, "Gluten Free" however the product contains wheat..
Details
Source
Food Recall
External ID
F-0891-2023
Action Date
2023-05-24
Status
Completed
Category
food
Product Description
Duke's SOUTHERN SAUCES BAYOU REMOULADE NET WT. 10 FL OZ (296 ml) GLUTEN FREE INGREDIENTS:***SOY SAUCE (WHEAT, SOYBEANS, AND SALT)***CONTAINS SOY, WHEAT, EGGS SAUER BRANDS, INC. RICHMOND, VA 23220 UPC x 52500 08582 7
Lot/Code Info: BEST BY 09/08/23 22346M 19 09:43
Quantity Affected: 340cs/9/10 fl oz bottles
Reason for Recall
The firm was notified by a consumer that the product label is incorrect. The label says, "Gluten Free" however the product contains wheat.
Distribution
Product was distributed to North Carolina & Ohio.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-17
Company
Richmond, VA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 74 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Sauer Brands, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sauer Brands, Inc. have FDA actions?
This is the only FDA action we have on record for Sauer Brands, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0891-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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