Drug recall
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint…
FDA recall event 65128 · Class I · Atlantic Pro Nutrients, Inc. dba XYMOGEN
Key facts
| Event ID | 65128 |
|---|---|
| Recall numbers | F-1523-2013 |
| Recalling firm | Atlantic Pro Nutrients, Inc. dba XYMOGEN |
| Product type | Food |
| Products | XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Undeclared Soy and Milk on the label. |
| Initiation date | May 1, 2013 |
| Report date | Jun 19, 2013 |
| Termination date | Jan 15, 2014 |
| City | Orlando |
| State | FL |
| Country | United States |
| FEI number | 3004315824 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: