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Atlantic Pro Nutrients, Inc. dba XYMOGEN recall — XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically…
FDA (enforcement) · June 19, 2013 · Class I
- Atlantic Pro Nutrients, Inc. dba XYMOGEN recalled XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support… — an FDA enforcement event posted , classified Class I, covering 1 product entry.
- FDA-stated reason: Undeclared Soy and Milk on the label.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- Atlantic Pro Nutrients, Inc. dba XYMOGEN
- Source ID
- 65128
FDA Enforcement Report search →
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-1523-2013 | XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles | All SKUs | AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY,… |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
Related: Undeclared-allergen recalls · Food recalls · All recall events