Food recall: all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
FDA enforcement event 64813 is a food recall by All One, Inc. of San Clemente, CA, initiated 28 Mar 2013 and classified Class II, with 2 product records.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 52% of the 546 food enforcement events initiated in 2013 carry the same class.
Status: Terminated, terminated 10 Jul 2014. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for All One, Inc..
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
All One, Inc., San Clemente, CA.
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."
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."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1339-2013 | all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters | 796 units | Class II | Terminated | 1 May 2013 |
| F-1340-2013 | all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters | 1,205 units | Class II | Terminated | 1 May 2013 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall 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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "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."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 10 Jul 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.