ModerateClass IITerminated

FDA Food recall · Reported May 1, 2013

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

Q: Which agency issued this recall?

This recall was issued by the FDA Food on May 1, 2013. Severity: Moderate. Recall number: F-1340-2013.

Q: Where was the recalled product distributed?

Distribution: 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..

Q: What are the health risks of consuming a recalled food product?

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

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.…

Recall #: F-1340-2013
Affected scope: 1,205 units
Initiated: March 28, 2013

Compiled from official public sources by the publisher. · Updated September 2026

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All One, Inc. recalled all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Sup… - a moderate-severity action.

all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Sup… was recalled by All One, Inc. in May 1, 2013. Reason: Product label misprinted to include claim of "No Dairy", even though milk is present in an ingredient (calciu…. Check the official notice for the remedy. Verify recall #F-1340-2013 with the FDA Food before acting.

The recall

All One, Inc. issued this moderate-severity FDA Food recall-Product label misprinted to include claim of "No Dairy", even though milk is present in an ingredient (calciu….

Moderate
severity level: 1K units
affected scope: Class II
classification: May 1, 2013
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1340-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

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

Reason for recall

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.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-1340-2013
Date reported	May 1, 2013
Date initiated	March 28, 2013
Recalling firm	All One, Inc.
Firm location	San Clemente, CA
Affected scope	1,205 units
Distribution	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.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

1,205 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall

Multi-state (10K – 100K units) -

Large-scale (100K – 1M units) -

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-1340-2013) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters. Recalled by All One, Inc.. Units affected: 1,205 units.

Why was this product recalled? ▼

Which agency issued this recall? ▼

This recall was issued by the FDA Food on May 1, 2013. Severity: Moderate. Recall number: F-1340-2013.

Where was the recalled product distributed? ▼

Distribution: 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..

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Similar Food · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

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Compare this recall with Grade A White In-shell Chicken eggs packaged in the followi… → · All Food recalls

This recall: FDA Food, reported May 1, 2013. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026