Enforcement Report - Week of September 12, 2012
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Event Detail
| Event ID | 62872 |
|---|---|
| Product Type | Food/Cosmetics |
| Status | Ongoing |
| Recalling Firm | Drucker Labs LP |
| City | Plano |
| State | TX |
| Country | US |
| Voluntary/Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2012-08-13 |
| Initial Firm Notification of Consignee or Public | Letter |
| Distribution Pattern | Nationwide and to Canada |
Product Detail
| Product Description | Code Info | Classification | Reason for Recall | Product Quantity | Recall Number |
|---|---|---|---|---|---|
| intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles | Lot 658 with a Best By date of 12/12 | Class II | 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 minutes and has no long-term side effects. | 2026 bottles | F-2126-2012 |
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