World’s Choice Products — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, World’s Choice Products has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 27 Apr 2016. World’s Choice Products is categorized under Beverages based on their predominant recall history.
Recall activity over time for World’s Choice Products
How serious are World’s Choice Products recalls?
FDA recall classifications by severity
Full FDA recall history for World’s Choice Products
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 27 Apr 2016Official FDA Notice | Choice Products Supreme Elixir 32oz. | Undeclared whey protein which contains milk and soy lecithin. | Class ITerminated |
| 27 Apr 2016Official FDA Notice | New Life Nature’s Blend 100% Multivitamin Juice 32oz. | Undeclared whey protein which contains milk and soy lecithin. | Class ITerminated |
| 27 Apr 2016Official FDA Notice | Choice Products. Xtreme Fiber Detox Net. Wt. 1lb Net Wt. 8oz. | Undeclared whey protein which contains milk and soy lecithin. | Class ITerminated |
Where have World’s Choice Products recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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