Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.
Tablets/Capsules Imprinted with Wrong ID
Consumers and healthcare providers should stop using this product immediately. Contact Unichem Pharmaceuticals USA Inc. or your healthcare provider for guidance. Notification method: Letter
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Doxazosin Tablets are prescribed primarily for managing high blood pressure and symptoms of BPH. Patients often rely on these medications for effective treatment.
The recall was initiated because the tablets were imprinted with incorrect identification. This could lead to confusion and potential misuse by patients.
This recall is not part of a broader industry pattern.
Consumers may face health risks if they continue using the recalled product. The need to consult healthcare providers and seek alternatives may cause delays in treatment.
The lot number can typically be found on the label of the bottle, along with the expiration date.
Expect a refund or replacement process to take approximately 4-6 weeks.
Keep records of your purchase receipt, any correspondence with the company, and photographs of the product.
The recall involves Doxazosin Tablets, USP, 4 mg, sold in 1000-tablet bottles. The affected lot is GDSH25006, with an expiration date of August 2027. These tablets were distributed nationwide.
Not sure what to do next? Our guide walks you through the process step by step.
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