Xymogen — 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, Xymogen has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 16 Aug 2013. Xymogen is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Xymogen
How serious are Xymogen recalls?
FDA recall classifications by severity
Full FDA recall history for Xymogen
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 16 Aug 2013Official FDA Notice | LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription Distributed by: PharmaceutiX Orlando, Florida | Product was labeled as a medical food as opposed to a dietary supplement. | Class IIITerminated |
| 16 Aug 2013Official FDA Notice | XYMOGEN LipiChol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by Xymogen Orlando, Florida. Also sold and distr | Product was labeled as a medical food as opposed to a dietary supplement. | Class IIITerminated |
| 1 May 2013Official FDA Notice | XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 1 | Undeclared Soy and Milk on the label. | Class ITerminated |
Where have Xymogen 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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