Recall Number: F-1523-2013
Why was XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles recalled?
Undeclared Soy and Milk on the label.
Check out this page for guidance on what to do if you've consumed food from recall F-1523-2013 .
City: Orlando
State: Florida
Country: United States
Classification: Class I
Classification Date: 2013-06-11
Reason: 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
Report Date: 2013-06-19
Product Type: Food
Status: Terminated
Recall Number: F-1523-2013
Postal Code: 32819-6544
Recall Initiation Date: 2013-05-01
Recall End Date: 2014-01-15
Event ID: 65128
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
Voluntary Or Mandated: Voluntary: Firm initiated
Initial Firm Notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Extra Info: All SKUs
Product Quantity: 16,268 units
Address: 6900 Kingspointe Pkwy
View Orlando, FL recalls.
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