Food recall

Atlantic Pro Nutrients, Inc. dba XYMOGEN recall: XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function

Atlantic Pro Nutrients, Inc. dba XYMOGEN, of Orlando, FL, recalled XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function. The FDA's reason: “Undeclared Soy and Milk on the label.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on May 1, 2013, and the FDA first listed it in its Enforcement Report of June 19, 2013. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed January 15, 2014

The recall

Company
Atlantic Pro Nutrients, Inc. dba XYMOGEN (Orlando, FL)
Reason, in FDA's words
“Undeclared Soy and Milk on the label.”
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
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
65128

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1523-2013 Class I

    XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles

    Codes: All SKUs

    Quantity: 16,268 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of June 19, 2013.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.