Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
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 Mylan Pharmaceuticals Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1186-2018 — Mylan Pharmaceuticals Inc. Mylan Pharmaceuticals Inc. recalls Diltiazem HCl Extended-Release Capsul Hello, I own a Mylan Pharmaceuticals Inc. recalls Diltiazem HCl Extended-Release Capsules, USP 120 mg 100-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, that is covered by recall D-1186-2018 from Mylan 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.
