Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit…
Liquid Assets Inc recalled this product and the FDA reported the enforcement action on 8 June 2016 as Class I. The recall was initiated by the firm. Dietary Supplements contain undeclared milk and soy.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant Derived Minerals 120 Capsules UPC: 0-16158-01225-3 Liquid Assets, Inc. Tulsa, OK 74116 1-888-497-4535 www.ExceptionalProducts.org; Magzuma Zuma Supreme Daily Wellness 147 Whole Food Nutrients Anti-aging and Superfruit Antioxidants 120 Vegetable Capsules Dietary Supplements, MagZuma, LLC. 7300 W. 110th St., Suite 700 Overland Park, Kansas 66210 TEL: 888.306.8855
- UPC
- 016158012253
- Reason for recall
- Dietary Supplements contain undeclared milk and soy.
- Recalling firm
- Liquid Assets Inc
- Firm location
- Tulsa, Oklahoma, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1405-2016
- Quantity
- 3145 bottles
- Distribution
- AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, Australia, Puerto Rico
- Initiated
- 20 April 2016
- Reported by FDA
- 8 June 2016
- Terminated
- 31 May 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot Numbers: 14656, 14657, 15109, 15489, 15488, 15616, and 16007
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
- The recall ran for 13 months, from 20 April 2016 to termination on 31 May 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 42 states, and the FDA published the enforcement report 7 weeks after the firm began the recall.
- Recalls of a dietary supplement run a median of 15 months, so this one was about typical for its category. Dietary supplements are regulated under their own good manufacturing practice rule, 21 CFR part 111, and they are the only food category where the dominant recall reason is an ingredient that was never declared because it is a pharmaceutical.
Named in the distribution pattern: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: milk, soy.
Filed under dietary supplements. A product can sit in more than one.
Every product in this recall
The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2016-06-08 | Life's Qik Fix 70 Plant Minerals Plus 80 Additional Nutrients 180 Vegetable Capsules Dietary Supplement Manufactured Exclusively For: MAGZUMA NUTRITION Overland Park, Kansas 66210 www.magzuma.com 1-888-306-8855 or 1-913-624-9676 | Liquid Assets Inc | Dietary Supplements contain undeclared milk and soy. | Class I |
Other dietary supplements recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Liquid Assets Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2016-06-08 | Life's Qik Fix 70 Plant Minerals Plus 80 Additional Nutrients 180 Vegetable Capsules Dietary Supplement Manufactured Exclusively For: MAGZUMA NUTRITION Overland Park, Kansas 66210 www.magzuma.com 1-888-306-8855 or 1-913-624-9676 | Liquid Assets Inc | Dietary Supplements contain undeclared milk and soy. | Class I |
All 2016 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.