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Class II: temporary or reversible health riskTerminated

Drucker Labs intraKID Lot 658 with a Best By date of 12/12 Recall

intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles

Drucker Labs LP · Plano, TX

Risk level
Class II
Reported by FDA
Sep 12, 2012
Recall ID
F-2126-2012
Check your lot numberHow we source this data

Summary

Drucker Labs recalled intraKID Lot 658 with a Best By date of 12/12 starting Aug 13, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2126-2012 on Sep 12, 2012. 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. Status: Terminated.

Why it was 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

Product description

intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles

Lot numbers, UPCs & expiration codes

Lot 658 with a Best By date of 12/12

Where it was sold

Nationwide and to Canada

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2126-2012
Classification
Class II
Status
Terminated
Recall initiated
Aug 13, 2012
FDA report date
Sep 12, 2012
Quantity
2026 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Drucker Labs LP

Original FDA data

Every field from FDA enforcement report F-2126-2012, exactly as published.

Show all FDA fields
City
Plano
State
TX
Status
Terminated
Country
United States
Event ID
62872
Address
1600 Capital Ave Ste 100
Code information
Lot 658 with a Best By date of 12/12
Postal code
75074-8187
Report date
Sep 12, 2012
Product type
Food
Recall number
F-2126-2012
Classification
Class II
Recalling firm
Drucker Labs LP
Product quantity
2026 bottles
Termination date
Oct 7, 2014
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
Voluntary / mandated
Voluntary: Firm initiated
Product description
intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
Distribution pattern
Nationwide and to Canada
Recall initiation date
Aug 13, 2012
Initial firm notification
Letter
Center classification date
Sep 5, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2126-2012, published Sep 12, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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