intraKID recall
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Why was intraKID recalled?
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
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 658 with a Best By date of 12/12
- Product
- intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
- Recalling firm
- Drucker Labs LP
- Quantity
- 2026 bottles
- Distribution
- Nationwide and to Canada
- Recall date
- September 12, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)