Subpotent Drug and Failed Impurities/Degradation Specifications
Subpotent Drug and Failed Impurities/Degradation Specifications
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 Institutional LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0413-2015 — Mylan Institutional LLC Mylan Institutional LLC recalls Nicardipine Hydrochloride Injection, 25 mg/ Hello, I own a Mylan Institutional LLC recalls Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India that is covered by recall D-0413-2015 from Mylan Institutional 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.
