Food Recall Check
Class III · Low risk Terminated Initiated Mar 22, 2012 (15 years ago)

Defense Nutrition Warrior Whey Natural Powder recall

Recalled by Defense Nutrition · Tarzana, CA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

The products contain undeclared soy lecithin

Undeclared allergen: 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

Defense Nutrition Warrior Whey Natural Powder, dietary supplement, packaged in 14-oz. bottles and packed 6/14-oz bottles per case.

Quantity: 10,380/14-oz bottles

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.

Lot numbers SP1094A2, Exp 04/04/2013; SP1153B2, Exp 06/02/2013; SP1319C2, Exp 11/15/2013 and SP2013C2, Exp 01/13/2014

Where it was sold

Alabama Arkansas Colorado Connecticut Florida Georgia Illinois Kansas Louisiana Maryland Michigan Minnesota Mississippi Nebraska Nevada New York Oregon Pennsylvania Tennessee Texas Utah Vermont Washington

FDA's distribution note: Distribution was made to IL, MI, MS, AL, CO, MD, TX, GA, NY, KS, AR, FL, NV, WA, CT, UT, VT, PA, LA, TN, NE, MN and OR. Foriegn distribution was made to Canada.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to 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
Defense Nutrition
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 22, 2012
In FDA report of
Aug 8, 2012
Terminated
Aug 14, 2013
FDA recall number
F-1813-2012 · event 61467
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Recent dietary supplements recalls

All dietary supplements recalls