Eden’s Answers — 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 22, 2026, Eden’s Answers has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 22 Sep 2022. Eden’s Answers is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Eden’s Answers
How serious are Eden’s Answers recalls?
FDA recall classifications by severity
Full FDA recall history for Eden’s Answers
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 22 Sep 2022Official FDA Notice | Sprigs – Honey Herbal Syrup: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case | High bacterial growth within products | Class IITerminated |
| 22 Sep 2022Official FDA Notice | Sprigs – Lil Ones Sleepy Time: Herbal Dietary Supplement 2oz glass amber bottles with black dropper, 12 units per case | High bacterial growth within products | Class IITerminated |
| 22 Sep 2022Official FDA Notice | Sprigs – Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case | High bacterial growth within products | Class IITerminated |
Where have Eden’s Answers 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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