Direct Rx recalls 5mg finasteride tablets with cGMP deviations. Affected lots expire 12/31/24. Consumers should check product details and contact manufacturer.
cGMP deviations
Direct Rx is recalling 5mg finasteride tablets due to manufacturing quality issues. This recall affects specific lots that expire by December 31, 2024. The issue could lead to unsafe drug products if not addressed.
The recall is due to cGMP deviations, which are manufacturing quality issues that could result in unsafe drug products. These deviations may affect the safety and effectiveness of the medication.
Men prescribed finasteride for conditions like enlarged prostate or hair loss who own the recalled lots. Those with the specific lot numbers 19AU2205 or 12OC2211 are most at risk.
Check for the lot numbers 19AU2205 or 12OC2211 on the packaging. The product is a 90-count bottle of 5mg finasteride tablets with an expiration date of December 31, 2024.
Look for the lot numbers 19AU2205 or 12OC2211 on the packaging of the 90-count finasteride tablets.
Direct Rx is recalling 5mg finasteride tablets with cGMP deviations in specific lots that expire by December 31, 2024.
Check for lot numbers 19AU2205 or 12OC2211 on the packaging of the 90-count finasteride tablets.
The recall record does not specify a remedy, so contact Direct Rx for further instructions.
We’ve drafted a message you can send Direct Rx to request your refund or repair — edit it as you like.
Subject: Recall D-0477-2023 — Direct Rx Direct Rx Hello, I own a Direct Rx that is covered by recall D-0477-2023 from Direct Rx. 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.
