Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
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 Aidarex Pharmaceuticals LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0990-2018 — Aidarex Pharmaceuticals LLC Aidarex Pharmaceuticals LLC recalls Enalapril Maleate, USP 2.5MG, 90-co Hello, I own a Aidarex Pharmaceuticals LLC recalls Enalapril Maleate, USP 2.5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. that is covered by recall D-0990-2018 from Aidarex 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.
