Why it was recalled
Undeclared Soy and Milk on the label.
Product description
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
Lot numbers, UPCs & expiration codes
All SKUs
Where it was 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 to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-1523-2013
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- May 1, 2013
- FDA report date
- Jun 19, 2013
- Quantity
- 16,268 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Atlantic Pro Nutrients, Inc. dba XYMOGEN
Original FDA data
Every field from FDA enforcement report F-1523-2013, exactly as published.
Show all FDA fields
- City
- Orlando
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 65128
- Address
- 6900 Kingspointe Pkwy
- Code information
- All SKUs
- Postal code
- 32819-6544
- Report date
- Jun 19, 2013
- Product type
- Food
- Recall number
- F-1523-2013
- Classification
- Class I
- Recalling firm
- Atlantic Pro Nutrients, Inc. dba XYMOGEN
- Product quantity
- 16,268 units
- Termination date
- Jan 15, 2014
- Reason for recall
- Undeclared Soy and Milk on the label.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
- Distribution pattern
- 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
- Recall initiation date
- May 1, 2013
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Jun 11, 2013