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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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Medium RiskFDA Food
Medications & Supplements/Dietary Supplements

Twenty-First Century Healthcare, Inc: Vitamin D3 Tablets Recalled Due to Potential High Dose Mislabeling

Agency Publication Date: May 20, 2021
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Summary

Twenty-First Century Healthcare, Inc. is recalling approximately 22,560 bottles of 21st Century Vitamin D3 125 mcg (5000 IU) tablets because a small portion of the bottles were mislabeled as a much lower 25 mcg (1000 IU) dose. Consumers taking these tablets based on the front label may unknowingly consume five times the amount of Vitamin D3 they intended. This recall affects 100-count bottles sold in Arizona, specifically those with lot number 15769204 and an expiration date of 01/24. Consumers should return the mislabeled product to the place of purchase for a full refund.

Risk

Mislabeled supplements can lead to accidental overconsumption of Vitamin D3, which may cause health complications if taken in excessive amounts over time. While the back label correctly identifies the high dose, the front label incorrectly lists it as a lower dose, creating a risk of dosing errors.

What You Should Do

  1. Check the front label of your 21st Century Vitamin D3 100-count bottle to see if it is labeled as 25 mcg (1000 IU).
  2. Verify the back label and the bottom of the bottle for Lot: 15769204 and Expiration Date: 01/24.
  3. Confirm the UPC code on the packaging is 7-40985-27431-6 to ensure it is the affected product.
  4. If the front label says 1000 IU but the back label or lot information matches the recalled product, stop using the supplement immediately.
  5. Return any affected bottles to the retail location where they were purchased for a full refund.
  6. Contact your healthcare provider or pharmacist if you have concerns about potential overconsumption of Vitamin D3.
  7. For further questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund for mislabeled product

How to: Return to the place of purchase for a full refund or contact the manufacturer for further instructions

Affected Products

Product: 21st Century Vitamin D3 125 mcg (5000 IU) tablet (100-count)
Item Code:
F-0543-2021
UPC Codes:
740985274316
Lot Numbers:
15769204 (Exp. 01/24)
Date Ranges: Expiration: 01/24

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87951
Status: Resolved
Manufacturer: Twenty-First Century Healthcare, Inc
Sold By: Retailers in Arizona
Manufactured In: United States
Units Affected: 22,560 bottles distributed; 2,425 identified with incorrect label
Distributed To: Arizona

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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.