Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
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 Valeant Pharmaceuticals North America LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0489-2019 — Valeant Pharmaceuticals North America LLC Valeant Pharmaceuticals North America LLC recalls Cardize Hello, I own a Valeant Pharmaceuticals North America LLC recalls Cardizem CD (diltiazem HCl) capsules, 240 mg, packaged in a) 30-count bottles (NDC 0187-0797-30); and b) 90-count that is covered by recall D-0489-2019 from Valeant Pharmaceuticals North America 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.
