WHY THIS PRODUCT IS LISTED
Other / see reason
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
Product description & recall reason
The recall record describes “intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles”; the source reports: “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.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- Lot 658 with a Best By date of 12/12
- Quantity
- 2026 bottles
Where it came from & where it went
- Recalling firm
- Drucker Labs LP
- Recalling firm address
- 1600 Capital Ave Ste 100; N/A; Plano; TX; 75074-8187; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- Nationwide and to Canada
States identified in the source
Nationwide — includes all U.S. states.
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.