Food Recall Check
Class I · High risk Terminated Initiated May 1, 2013 (13 years ago)

XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen… recall

Recalled by Atlantic Pro Nutrients, Inc. dba XYMOGEN · Orlando, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared Soy and Milk on the label.

Undeclared allergens: Milk Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 16,268 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

All SKUs

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina New Jersey New Mexico New York Ohio Oklahoma Pennsylvania Rhode Island South Carolina Tennessee Texas Utah Virginia Washington Wisconsin West Virginia Wyoming

FDA's distribution note: 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

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Atlantic Pro Nutrients, Inc. dba XYMOGEN
Initiated by
Voluntary: Firm initiated
Recall initiated
May 1, 2013
In FDA report of
Jun 19, 2013
Terminated
Jan 15, 2014
FDA recall number
F-1523-2013 · event 65128
Official record
FDA enforcement report search

Other recalls by Atlantic Pro Nutrients, Inc. dba XYMOGEN

Class III · Low risk Terminated Labeling

LipiChol 540

Reason Product was labeled as a medical food as opposed to a dietary supplement.

Atlantic Pro Nutrients, Inc. dba XYMOGEN Nationwide F-0816-2014
Class III · Low risk Terminated Labeling

XYMOGEN LipiChol

Reason Product was labeled as a medical food as opposed to a dietary supplement.

Atlantic Pro Nutrients, Inc. dba XYMOGEN Nationwide F-0815-2014

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