The Recall Desk
ModerateFDA (Food)·F-2126-2012·Announced 2012-09-12

Drucker Labs Recalls intraKID Due to Incorrect Vitamin B3 Form

Drucker Labs is recalling intraKID Lot 658 because it was manufactured with an incorrect form of Vitamin B3, which may cause temporary skin symptoms.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text describes the hazard as a temporary, self-limiting symptom (Niacin Flush) without reports of hospitalization or serious injury, fitting the Moderate criteria for low-risk contamination or minor issues.

Plain-English summary

Drucker Labs LP is recalling 2,026 bottles of intraKID, Lot 658, with a Best By date of 12/12. The affected products are available in 33 oz and 2 oz bottles. The recall covers distribution nationwide and to Canada.

The recall was initiated after testing and investigation determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used during manufacturing. This specific nutrient may cause a temporary symptom known as Niacin Flush in a small number of consumers. Symptoms may include itching, redness, or warmth of the skin, which typically subsides within 15 to 20 minutes.

Consumers who have purchased this specific lot should stop using the product and contact Drucker Labs for further instructions.

The recalled product

Product
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Manufacturer
Drucker Labs LP
Category
Food — Dietary Supplement
Hazard
Affected units
2,026

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot 658 with a Best By date of 12/12

Distribution

Distributed nationwide across the United States.

Related recalls

Same hazard · incorrect ingredient

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