Northwind Pharmaceuticals recalls 20mg Tadalafil tablets due to manufacturing quality issues. Affected lots expire by November 2023. Consumers should check product labels for specific lot numbers and expiration dates.
CGMP Deviations
Northwind Pharmaceuticals is recalling 20mg Tadalafil tablets that were repackaged by their company. The recall is due to CGMP (Current Good Manufacturing Practice) deviations, which means the product may not meet safety standards. This recall affects people who have these specific bottle sizes and lot numbers.
CGMP deviations refer to failures in the manufacturing process that could affect the product's safety and quality. These deviations mean the tablets might not meet the required standards for safe use, but the specific risk is not described as causing serious injury in normal use.
People who have the 6-count or 15-count bottles of Tadalafil Tablets, USP 20mg with the listed lot numbers and expiration dates are affected. Those who use prescription medications for erectile dysfunction are most at risk.
Check the product label for the lot number and expiration date. The affected products are 6-count or 15-count bottles with lot numbers F113892001-F113892203 and expiration dates up to November 2023.
Look for the lot number and expiration date on the bottle to determine if it is affected.
The recall is due to CGMP deviations, which means the product may not meet safety and quality standards during manufacturing.
Check the product label for the lot number and expiration date. If it matches the affected lots listed, contact Northwind Pharmaceuticals for instructions.
The recall is for manufacturing quality issues, but the specific risk is not described as causing serious injury in normal use.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0553-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0553-2023 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.
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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.
