Status
Terminated
Food Enforcement F-2126-2012
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
Classification
Class II
Report Date
September 12, 2012
Recall Initiation
August 13, 2012
Product Information
- Product description
- intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
- Product quantity
- 2026 bottles
- Product type
- Food
- 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
- Initial firm notification
- Letter
- Distribution pattern
- Nationwide and to Canada
Location & Firm
- Recalling firm
- Drucker Labs LP
- Address
-
1600 Capital Ave Ste 100, N/A
United States - Voluntary / Mandated
- Voluntary: Firm initiated
Codes & Dates
- Recall number
- F-2126-2012
- Event ID
- 62872
- Recall initiation date
- August 13, 2012
- Center classification date
- September 5, 2012
- Code info
- Lot 658 with a Best By date of 12/12
- More code info
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