Accord Healthcare recalls Doxazosin 2mg tablets (NDC 16729-414-01) following FDA inspection for manufacturing deviations. Consumers should check product details and contact the manufacturer for instructions.
CGMP Deviations: recalling drug products following an FDA inspection.
Accord Healthcare is recalling Doxazosin 2mg tablets due to manufacturing deviations found during an FDA inspection. This recall affects specific packaging and batch numbers, and consumers should check their product details to determine if they are affected.
The recall is due to manufacturing deviations identified by the FDA during an inspection. This means the drug may not meet quality standards, but the specific risk to consumers is not clearly described in the recall notice.
People who have the recalled Doxazosin tablets (100-count or 1,000-count bottles) from specific batch numbers and expiration dates. Those with prescriptions for this medication are most at risk.
Check for the 100-count bottle (NDC 16729-414-01) or 1,000-count bottle (NDC 16729-414-17) with specific batch numbers and expiration dates listed in the recall notice.
Identify the product by checking the NDC number, batch number, and expiration date on the packaging.
The FDA found manufacturing deviations during an inspection, which means the drug may not meet quality standards.
The recalled products are Doxazosin 2mg tablets in 100-count bottles (NDC 16729-414-01) and 1,000-count bottles (NDC 16729-414-17) with specific batch numbers and expiration dates.
The recall notice does not specify a stop-use instruction, so consumers should check the product details and contact the manufacturer for further instructions.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0387-2023 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0387-2023 from Accord Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
