FDA recalls · F-0101-2014
Vitalab Co Inc recall
- FoodVIT-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
- ReasonThe firm reports a customer found a foreign object in the product.
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2014-09-11
- DatesFirm started it 2013-10-04. In FDA's enforcement report 2013-11-13.
- Sold inDistribution 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.
- Amount280 bottles
- CodesAll three labels have the same lot code: 06-11-15-2
- FirmVitalab Co Inc, Kansas City, MO · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-0101-2014. Class meanings: FDA.