cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.
cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.
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 Jubilant Cadista Pharmaceuticals, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-296-2013 — Jubilant Cadista Pharmaceuticals, Inc. Jubilant Cadista Pharmaceuticals Inc. recalls Pantoprazole So Hello, I own a Jubilant Cadista Pharmaceuticals Inc. recalls Pantoprazole Sodium Delayed Release Tablets USP, 40 mg, 90 count bottles, Manufactured by Jubilant Life Sciences Ltd, that is covered by recall D-296-2013 from Jubilant Cadista Pharmaceuticals, Inc.. 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.
