F-0101-2014 Class II Terminated
FDA food recall F-0101-2014 was initiated by Vitalab Co Inc on October 4, 2013 and is designated Class II. Reason for recall: The firm reports a customer found a foreign object in the product. The recall status is terminated (terminated September 11, 2014). Affected quantity: 280 bottles.
Recall Details
- Product Type
- Food
- Report Date
- November 13, 2013
- Initiation Date
- October 4, 2013
- Termination Date
- September 11, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 280 bottles
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
Reason for Recall
The firm reports a customer found a foreign object in the product.
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.
Code Information
All three labels have the same lot code: 06-11-15-2