Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
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 Cipla Limited to request your refund or repair — edit it as you like.
Subject: Recall D-1078-2015 — Cipla Limited Cipla Limited recalls Levalbuterol Inhalation Solution, USP, 0.31 mg/ 3 mL, 3 mL Vial Hello, I own a Cipla Limited recalls Levalbuterol Inhalation Solution, USP, 0.31 mg/ 3 mL, 3 mL Vials, Rx Only. Manufactured by: Cipla Ltd. Plot 9 & 10, that is covered by recall D-1078-2015 from Cipla Limited. 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.
