Accord Healthcare recalls 1 mg Finasteride tablets due to FDA inspection findings. Products with NDC 16729-089-10 or 16729-089-15 may be affected. No specific remedy provided in recall notice.
CGMP Deviations: recalling drug products following an FDA inspection.
Accord Healthcare is recalling 1 mg Finasteride tablets that were manufactured following an FDA inspection. This recall is due to compliance issues identified during the inspection, but no specific safety risk is described in the notice.
The recall is triggered by FDA inspection findings indicating compliance issues with the manufacturing process. However, the notice does not specify any safety hazards or risks to consumers from the product.
Prescription holders of the recalled Finasteride tablets may be affected. Patients using the product for medical treatment are most at risk if they have the specific batch numbers listed.
Check for the NDC code 16729-089-10 (30-count bottle) or 16729-089-15 (90-count bottle) on the product label. The product was manufactured by Intas Pharmaceuticals in India and distributed by Accord Healthcare in the US.
Identify the NDC code on the product label to confirm if it matches the recalled items.
The recall is due to FDA inspection findings indicating compliance issues with the manufacturing process, but no specific safety risk is described in the notice.
The recall notice does not specify any action steps for consumers. Check the product details to see if it matches the recalled items.
The recall notice does not describe any safety hazards or risks to consumers from the product.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0390-2023 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0390-2023 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.
