Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
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 AstraZeneca LP to request your refund or repair — edit it as you like.
Subject: Recall D-199-2013 — AstraZeneca LP AstraZeneca LP recalls PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Hello, I own a AstraZeneca LP recalls PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989-04 that is covered by recall D-199-2013 from AstraZeneca LP. 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.
