FDA Food recall F-0101-2014
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber bottles
- FDA Food
- Class II
- terminated
- Published 2013-11-13
On 2013-11-13 the FDA classified a Class II recall of VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber bottles by Vitalab, citing the firm reports a customer found a foreign object in the product.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0101-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-04 |
| Published | 2013-11-13 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Vitalab |
| Distribution | AZ, CA, CO, FL, GA, IA, IL, KS, KY, LA, MD, MI, MN, MO, NC, NE, NH, NJ, NY, OH, OR, PA, PR, TX, WA, WI |
Product
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
The firm reports a customer found a foreign object in the product.
Identifiers
| code_info | All three labels have the same lot code: 06-11-15-2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0101-2014%22
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