Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported March 14, 2018
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Vitalab Co Inc recalled Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Diet… - a moderate-severity action.
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Diet… was recalled by Vitalab Co Inc in March 14, 2018. Reason: The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the…. Check the official notice for the remedy. Verify recall #F-0883-2018 with the FDA Food before acting.
The recall
Vitalab Co Inc issued this moderate-severity FDA Food recall-The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the….
- Moderate
- severity level
- Class II
- classification
- March 14, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0883-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0883-2018) was formally reported on March 14, 2018, with the manufacturer initiating the action on February 8, 2018. 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 1,703 bottles.
The documented reason for this recall is: The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label. Distribution data in the federal record shows the product reached: Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada.. 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, 2 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.
Food recalls over time
Where this recall sits in its category - 25,126 food 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
1,703 bottles
Related Recalls
6
2 from same agency
Product description
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;
Reason for recall
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0883-2018 |
| Date reported | March 14, 2018 |
| Date initiated | February 8, 2018 |
| Recalling firm | Vitalab Co Inc |
| Firm location | Kansas City, MO |
| Affected scope | 1,703 bottles |
| Distribution | Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada. |
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-0883-2018) 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? ▼
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;. Recalled by Vitalab Co Inc. Units affected: 1,703 bottles.
Why was this product recalled? ▼
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 14, 2018. Severity: Moderate. Recall number: F-0883-2018.
Where was the recalled product distributed? ▼
Distribution: Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0883-2018) 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.
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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 March 14, 2018. 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.