XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically… — Class I food recall F-1523-2013
Terminated recall by Atlantic Pro Nutrients, Inc. dba XYMOGEN, reported 2013-06-19, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Undeclared Soy and Milk on the label.
| Recall number | F-1523-2013 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atlantic Pro Nutrients, Inc. dba XYMOGEN, Orlando, FL, United States |
| Recall initiated | 2013-05-01 |
| Classified | 2013-06-11 |
| Reported by FDA | 2013-06-19 |
| Terminated | 2014-01-15 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY |
| Quantity | 16,268 units |
| Reason classes | undeclared allergen, labeling |
| Allergens | milk, soy |
Product
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
Reason for recall
Undeclared Soy and Milk on the label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1523-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.