FDA Food recall · Reported September 12, 2012
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. Th…
Drucker Labs LP recalled intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles - a moderate-severity action.
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles was recalled by Drucker Labs LP in September 12, 2012. Reason: After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, …. Check the official notice for the remedy. Verify recall #F-2126-2012 with the FDA Food before acting.
The recall
Drucker Labs LP issued this moderate-severity FDA Food recall-After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, ….
- Moderate
- severity level
- Class II
- classification
- September 12, 2012
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2126-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,371 cosmetics & personal care recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Reason for recall
After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. This nutrient may cause a temporary symptom in a small number of consumers. This symptom, commonly known as Niacin Flush, may include itching, redness, or warmth of the skin. This typically subsides within 15 20 minut
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2126-2012 |
| Date reported | September 12, 2012 |
| Date initiated | August 13, 2012 |
| Recalling firm | Drucker Labs LP |
| Firm location | Plano, TX |
| Affected scope | 2026 bottles |
| Distribution | Nationwide and to 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-2126-2012) 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? ▼
Why was this product recalled? ▼
Which agency issued this recall? ▼
Where was the recalled product distributed? ▼
What are the health risks of consuming a recalled food product? ▼
Nationwide recalls with similar severity or category timing
Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Cosmetics & Personal Care · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 7… → · All Cosmetics & Personal Care recalls
Methodology · Corrections · Archive as of August 2026