Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 28, 2013 (14 years ago)

all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement recall

Recalled by All One, Inc. · San Clemente, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product label misprinted to include claim of "No Dairy", even though milk is present in an ingredient (calcium caseinate). "Certified Vegan" is also claimed on the product label. The side panel discusses the presence of milk in the product.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters

Quantity: 1,205 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.

UPC: 0 52534 20001 2, Lot No. 172801, Use By: 10/14.

Where it was sold

Nationwide.

Alaska Alabama Arkansas Arizona California Colorado Florida Georgia Hawaii Indiana Kansas Kentucky Louisiana Maryland Maine Michigan Missouri Mississippi North Carolina Nebraska New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin Wyoming

FDA's distribution note: Nationwide including: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IN, KY, KS, LA, ME, MD, MI, MO, MS, NC, NJ, NM, NE, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI and WY.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
All One, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 28, 2013
In FDA report of
May 1, 2013
Terminated
Jul 10, 2014
FDA recall number
F-1340-2013 · event 64813
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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