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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 Drug
Medications & Supplements/Prescription Drugs

Unichem Doxazosin Tablets Recalled for Incorrect Imprint Identification

Agency Publication Date: February 11, 2026
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Summary

Unichem Pharmaceuticals USA Inc. is recalling approximately 60,000 bottles of Doxazosin Tablets (4 mg) because the tablets or capsules are imprinted with the wrong identification code. This prescription medication is used to treat high blood pressure and symptoms of an enlarged prostate. Consumers should check their prescription bottles to see if they have the affected lot GDSH25006 with an expiration date of August 2027.

Risk

The wrong imprint on a medication can lead to a patient taking the incorrect drug or dosage, which may result in ineffective treatment of their condition or unexpected side effects. Because this is a low-risk (Class III) recall, the health consequences are unlikely to be severe, but accurate pill identification is critical for patient safety.

What You Should Do

  1. Check your medication bottle for Doxazosin Tablets, 4 mg, with NDC 29300-353-10, Lot GDSH25006, and an expiration date of 08/2027.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Doxazosin Tablets, USP (1000 tablets per bottle)
Variants: 4 mg, Rx only
Lot Numbers:
GDSH25006 (Exp 08/2027)
NDC:
29300-353-10

Distributed by Unichem Pharmaceuticals (USA), Inc. and manufactured by Unichem Laboratories Limited (India).

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98321
Status: Active
Manufacturer: Unichem Pharmaceuticals USA Inc.
Manufactured In: United States, India
Units Affected: 60,000 tablets
Distributed To: Nationwide

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.