Preferred Pharmaceuticals recalls 5mg Finasteride tablets due to manufacturing quality deviations at Accord Healthcare. Products with specific NDC codes and expiration dates are affected. Consumers should contact the company for details.
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Preferred Pharmaceuticals is recalling 5mg Finasteride tablets that were manufactured by Accord Healthcare. The recall is due to quality control issues found during manufacturing inspections. This affects specific product batches with certain NDC codes and expiration dates.
The recall is based on manufacturing quality deviations detected at Accord Healthcare during inspections. This means the tablets may not meet the required quality standards, but the specific health risks are not detailed in the recall notice.
Men prescribed Finasteride for conditions like benign prostatic hyperplasia (BPH) who own the recalled 5mg tablets. Those with specific NDC codes and expiration dates listed in the recall are most at risk.
Check for 30-count or 90-count bottles with NDC codes 68788-6976-3 or 68788-6976-9. The products have specific expiration dates listed in the recall notice.
Identify the NDC code and expiration date on the bottle to confirm if it matches the recalled items.
The recall is due to manufacturing quality deviations found at Accord Healthcare during inspections.
The recall notice does not specify a remedy; you should check the product details and contact Preferred Pharmaceuticals for further instructions.
Yes, the recalled products have specific expiration dates including 8/31/2023, 5/31/2024, 10/31/2023, and 11/30/2024.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0516-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0516-2023 from Preferred Pharmaceuticals. 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.
