CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Northwind Pharmaceuticals LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1098-2018 — Northwind Pharmaceuticals LLC Northwind Pharmaceuticals LLC recalls Valsartan, 320mg, 30 tablets pe Hello, I own a Northwind Pharmaceuticals LLC recalls Valsartan, 320mg, 30 tablets per bottle, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. that is covered by recall D-1098-2018 from Northwind Pharmaceuticals LLC. 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.
