purely elizabeth — 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, purely elizabeth has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 2 Jan 2020. purely elizabeth is categorized under Snacks & Candy based on their predominant recall history.
Recall activity over time for purely elizabeth
How serious are purely elizabeth recalls?
FDA recall classifications by severity
Full FDA recall history for purely elizabeth
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 2 Jan 2020Official FDA Notice | purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 oz (227g). UPC 55140-00268. Made with organic quinoa | Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags. | Class IITerminated |
| 29 Mar 2018Official FDA Notice | Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case, | Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin. | Class IITerminated |
| 17 Nov 2016Official FDA Notice | Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case, | Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin. | Class IITerminated |
Where have purely elizabeth 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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