Product packaged in the following ways A) Sonne's
Reason The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
VIT-RA-TOX Whole Beet Plant Juice recall
Recalled by Vitalab Co Inc · Kansas City, MO, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The firm reports a customer found a foreign object in the product.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber bottles. No. 48. National Distributors: V.E. Irons, Inc, N. Kansas City, MO. Springreen Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber bottles. No. 88. National Distributors: Springreen Products, Inc, N. Kansas City, MO. Sonne's Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber bottles. No. 18. National Distributors: Sonne's Organic Foods, Inc., N. Kansas City, MO
Quantity: 280 bottles
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.
All three labels have the same lot code: 06-11-15-2
Where it was sold
Arizona California Colorado Florida Georgia Iowa Illinois Kansas Kentucky Louisiana Maryland Michigan Minnesota Missouri North Carolina Nebraska New Hampshire New Jersey New York Ohio Oregon Pennsylvania Puerto Rico Texas Washington Wisconsin
FDA's distribution note: Distribution was made both retail and wholesale to AZ, CA, CO, FL, GA, IA, IL, KS, KY, LA, MD, MI, MN, NJ, MN, MO, NC, NE, NH, NY, OH, OR, PA, TX, WA and WI. Distribution was made to PR.
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
- Vitalab Co Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 4, 2013
- In FDA report of
- Nov 13, 2013
- Terminated
- Sep 11, 2014
- FDA recall number
- F-0101-2014 · event 66446
- Official record
- FDA enforcement report search
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