Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 4, 2013

VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150…

Recalling firm: Vitalab Co Inc

Why it was recalled

The firm reports a customer found a foreign object in the product.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 11, 2014.

Check your package

Compare the exact product and package details with the label you have.

ProductVIT-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

FDA code information

All three labels have the same lot code: 06-11-15-2

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
lot06-11-15-2All three labels have the same lot code: 06-11-15-2

Original FDA recall reason

The firm reports a customer found a foreign object in the product.

Recall details

Recall number
F-0101-2014
Event ID
66446
FDA status
Terminated
Initiated
Oct 4, 2013
Reported
Nov 13, 2013
Classified
Nov 1, 2013
Terminated
Sep 11, 2014
Quantity
280 bottles
Location
Kansas City, MO, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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.

FDA source record · F-0101-2014

Data updated September 16, 2026. View official FDA data ↗

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