Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported November 13, 2013
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,
The firm reports a customer found a foreign object in the product.
Vitalab Co Inc recalled VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 1… - a moderate-severity action.
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 1… was recalled by Vitalab Co Inc in November 13, 2013. Reason: The firm reports a customer found a foreign object in the product.. Check the official notice for the remedy. Verify recall #F-0101-2014 with the FDA Food before acting.
The recall
Vitalab Co Inc issued this moderate-severity FDA Food recall-The firm reports a customer found a foreign object in the product..
- Moderate
- severity level
- Class II
- classification
- November 13, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0101-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0101-2014) was formally reported on November 13, 2013, with the manufacturer initiating the action on October 4, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Vitalab Co Inc is listed as the recalling firm, operating out of Kansas City, MO. Federal records list the affected scope as 280 bottles.
The documented reason for this recall is: The firm reports a customer found a foreign object in the product. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
280 bottles
Related Recalls
6
1 from same agency
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0101-2014 |
| Date reported | November 13, 2013 |
| Date initiated | October 4, 2013 |
| Recalling firm | Vitalab Co Inc |
| Firm location | Kansas City, MO |
| Affected scope | 280 bottles |
| Distribution | 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. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0101-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Vitalab Co Inc. Units affected: 280 bottles.
Why was this product recalled? ▼
The firm reports a customer found a foreign object in the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 13, 2013. Severity: Moderate. Recall number: F-0101-2014.
Where was the recalled product distributed? ▼
Distribution: 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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0101-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 13, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.