Northwind Pharmaceuticals recalls 4mg Doxazosin tablets due to CGMP deviations. Affected lots: F107752201, expiring 05/31/2024. No specific remedy stated in recall notice.
CGMP Deviations
Northwind Pharmaceuticals is recalling 4mg Doxazosin tablets that were repackaged by their company. The recall is due to CGMP deviations, which means the manufacturing process didn't meet quality standards. This could affect safety, but the recall notice doesn't specify what to do with the product.
CGMP deviations refer to failures in the manufacturing process that could lead to unsafe products. These deviations might affect the tablet's quality, but the recall notice doesn't specify the exact risk to health.
Prescription holders of the 4mg Doxazosin tablets repackaged by Northwind Pharmaceuticals in Indianapolis, IN. Most at risk are those who have the specific lot number F107752201.
Check for the product name 'Doxazosin Tablets, USP, 4mg, 30-count bottles' with the lot number F107752201 and expiration date 05/31/2024. The product was repackaged by Northwind Pharmaceuticals in Indianapolis, IN.
Look for the lot number F107752201 and expiration date 05/31/2024 on the packaging.
The recall is due to CGMP deviations, which means the manufacturing process didn't meet quality standards.
The recall notice does not specify a remedy, so no action is required beyond checking the product details.
The recall notice does not describe a specific hazard that could cause injury.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0550-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0550-2023 from Northwind 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.