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RECALL RECORD — CLASS IIRecall closedF-1340-2013/FDA enforcement
All One, INC.·Dietary Supplements·Mar 28, 2013

All One Original Formula Multiple Vitamin & Mineral Powder Dietary Supplement, 30 Day Supply, …

What you need to know

Class II

  • What happened

    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…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameAll One, INC.
Recalling firmAll One, INC.San Clemente, CA, United States
UPC / barcodes
0 52534 20001 2
Lot / date codes
  • UPC: 0 52534 20001 2, Lot No. 172801, Use By: 10/14.
Distribution area
Nationwide

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.

United States

Quantity affected1, 205 units
Recall initiationFDA report date: May 1, 2013
FDA recall numberF-1340-2013

Beyond the headline

The recall, in context

All One, INC. initiated this supplements recall on March 28, 2013. The FDA enforcement report states: 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. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: 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.

All One Original Formula Multiple Vitamin & Mineral Powder Dietary Supplement, 30 Day Supply, … was made or distributed by All One, INC. in San Clemente, CA, United States. This page reflects FDA report F-1340-2013, dated May 1, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the All One Original Formula Multiple Vitamin & Mineral Powder Dietary Supplement, 30 Day Supply, … recall?

All One, INC. recalled All One Original Formula Multiple Vitamin & Mineral Powder Dietary Supplement, 30 Day Supply, … in an FDA Class II enforcement action reported as F-1340-2013. 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…

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the All One, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1340-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by All One, INC.

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All One, INC.

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Product label misprinted to include claim of "No Dairy", even though milk is present in an ingredient (whey protein isolate). "Certified Vegan" is also claimed on the product…

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.