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Class II: temporary or reversible health riskTerminated

Vitalab VIT-RA-TOX Whole Beet Plant Juice Recall

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

Vitalab Co Inc · Kansas City, MO

Risk level
Class II
Reported by FDA
Nov 13, 2013
Recall ID
F-0101-2014
Check your lot numberHow we source this data

Summary

Vitalab recalled VIT-RA-TOX Whole Beet Plant Juice starting Oct 4, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0101-2014 on Nov 13, 2013. Reason: The firm reports a customer found a foreign object in the product. Status: Terminated.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0101-2014
Classification
Class II
Status
Terminated
Recall initiated
Oct 4, 2013
FDA report date
Nov 13, 2013
Quantity
280 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Vitalab Co Inc

Original FDA data

Every field from FDA enforcement report F-0101-2014, exactly as published.

Show all FDA fields
City
Kansas City
State
MO
Status
Terminated
Country
United States
Event ID
66446
Address
705 Mcgee St
Code information
All three labels have the same lot code: 06-11-15-2
Postal code
64106-1607
Report date
Nov 13, 2013
Product type
Food
Recall number
F-0101-2014
Classification
Class II
Recalling firm
Vitalab Co Inc
Product quantity
280 bottles
Termination date
Sep 11, 2014
Reason for recall
The firm reports a customer found a foreign object in the product.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
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.
Recall initiation date
Oct 4, 2013
Initial firm notification
Letter
Center classification date
Nov 1, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0101-2014, published Nov 13, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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