Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016, 12 retail units per wholesale case
Summary
The FDA issued a Class III for Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016, 12 retail units per by SUBCO FOODS INC. Reason: Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and.
Details
Source
Food Recall
External ID
F-1705-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016, 12 retail units per wholesale case
Lot/Code Info: Lot #24128
Quantity Affected: 256 cases
Reason for Recall
Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.
Distribution
CT, DE, MD, NJ, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-09
Company
West Chicago, IL
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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SUBCO FOODS INC has 2 FDA actions in our database, including 2 recalls.
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 (SUBCO 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 SUBCO FOODS INC have FDA actions?
SUBCO FOODS INC 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-1705-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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