Northwind Pharmaceuticals recalls 10mg Atorvastatin tablets due to CGMP deviations. Affected lots may have quality issues; contact for details.
CGMP Deviations
Northwind Pharmaceuticals is recalling 10mg Atorvastatin Calcium Tablets in 30-count bottles that were repackaged by their company. This recall is due to deviations in current good manufacturing practices (CGMP), which could affect product quality.
CGMP deviations refer to failures in the manufacturing process that could lead to product quality issues. These deviations may result in tablets that do not meet safety or effectiveness standards, though the specific risk is not detailed in the recall notice.
Prescription holders of the 10mg Atorvastatin Calcium Tablets, 30-count bottles repackaged by Northwind Pharmaceuticals. People taking this medication for cholesterol management are most at risk.
Check for the product name 'Atorvastatin Calcium Tablets, USP, 10 mg, 30-count bottles' repackaged by Northwind Pharmaceuticals. Look for NDC code 51655-946-52 and lot number F117192201 with an expiration date of 4/30/2023.
Identify the product by checking the NDC code 51655-946-52 and lot number F117192201 on the packaging.
The recall is due to CGMP deviations, which are manufacturing process failures that could affect product quality.
The recall notice does not specify a remedy, so contact Northwind Pharmaceuticals for further instructions.
The recall does not mention any specific safety hazards or injuries, so the risk is unknown.
We’ve drafted a message you can send Northwind Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0548-2023 — Northwind Pharmaceuticals Northwind Pharmaceuticals Hello, I own a Northwind Pharmaceuticals that is covered by recall D-0548-2023 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.
