CLASS I Food recall · Reported 19 Jun 2013 · FDA Enforcement Report
Xymogen EP Exclusive Patented Dietary Supplement Artriphen recalled
Atlantic Pro Nutrients is recalling Xymogen EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support, distributed in 41 states. The recall was initiated on 1 May 2013 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1523-2013
- FDA event ID
- 65128
- Recalling firm
- Atlantic Pro Nutrients, Orlando, FL
- Brand
- Xymogen EP
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 1 May 2013
- FDA classified
- 11 Jun 2013
- Reported
- 19 Jun 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Milk
- Product category
- Dietary Supplements
Timeline
| 1 May 2013 | Recall initiated by company | |
| 11 Jun 2013 | Classified by FDA | +41 days |
| 19 Jun 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Soy and Milk on the label.
Product as listed by the FDA
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
Where it was distributed
AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, 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, District of Columbia and Hawaii
AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaHawaiiIowaIllinoisKansasKentuckyLouisianaMassachusettsMarylandMaine
Questions about this recall
Why was it recalled?
Undeclared Soy and Milk on the label.
Which lots are affected?
All SKUs
Where was it sold?
AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, 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, District of Columbia and Hawaii
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Atlantic Pro Nutrients
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS III | Xymogen LipiChol (Omega-3 Phospholipid 540 mg) Medical Food recalledXymogen LipiChol | Atlantic Pro Nutrients | Other | Nationwide |
| Food | CLASS III | LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense recalledLipiChol | Atlantic Pro Nutrients | Other | Nationwide |
Other Dietary Supplements recalls
All 733| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |