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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Dietary Supplements

Healthprint Vitamin D3 5000 Recalled for Sub-potency and Mislabeling

Agency Publication Date: February 26, 2024
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Summary

Ancient Formulas, Inc. is recalling 111 bottles of Healthprint Vitamin D3 5000 Dietary Supplement (200 tablets) due to a sub-potency issue. Testing revealed that the product contains less Vitamin D than indicated on the bottle, and the label contains an incorrect percent daily value for the nutrient. No incidents or injuries have been reported to date in connection with this recall.

Risk

The product is sub-potent, meaning it contains significantly less Vitamin D than listed on the nutrition label. Consumers taking this product may not receive the intended nutritional benefit, and the incorrect daily value percentage on the label provides misleading information about the supplement's strength.

What You Should Do

  1. This recall affects Healthprint Vitamin D3 5000 Dietary Supplement (200 tablets) packaged in plastic bottles and marked with lot number 063-0723.
  2. Return the product to the place of purchase for a refund, throw it away, or contact Ancient Formulas, Inc. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have questions or wish to report a concern.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Healthprint Vitamin D3 5000 Dietary Supplement (200 tablets)
Variants: 200 tablets, Plastic bottle
Lot Numbers:
063-0723

Recall number: F-0930-2024; Total quantity distributed: 111 bottles.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93899
Status: Resolved
Manufacturer: Ancient Formulas, Inc.
Sold By: Ancient Formulas, Inc.
Manufactured In: United States
Units Affected: 111 bottles
Distributed To: Florida

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.