Mehlenbacher’s Taffy — 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, Mehlenbacher’s Taffy has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 20 Jul 2023. Mehlenbacher’s Taffy is categorized under Produce based on their predominant recall history.
Recall activity over time for Mehlenbacher’s Taffy
How serious are Mehlenbacher’s Taffy recalls?
FDA recall classifications by severity
Full FDA recall history for Mehlenbacher’s Taffy
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 20 Jul 2023Official FDA Notice | Mehlenbacher’s Taffy, 1.25 oz per piece, 36 pieces/box, cello wrapped. Watermelon UPC 022099174004. Storage in a cool dr | Undeclared allergen; milk | Class IITerminated |
| 20 Jul 2023Official FDA Notice | Mehlenbacher’s Taffy, 1.25 oz per piece, 36 pieces/box, cello wrapped. Strawberry lemonade UPC 022099174035. Storage in | Undeclared allergen; milk | Class IITerminated |
| 20 Jul 2023Official FDA Notice | Mehlenbacher’s Taffy, 1.25 oz per piece, 36 pieces/box, cello wrapped. Peanut butter cup, UPC 022099174080. Storage in a | Undeclared allergen; milk | Class IITerminated |
Where have Mehlenbacher’s Taffy recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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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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