Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).
Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).
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 Pharmaceuticals LP to request your refund or repair — edit it as you like.
Subject: Recall D-0585-2018 — AstraZeneca Pharmaceuticals LP AstraZeneca Pharmaceuticals LP recalls Lynparza (olaparib) capsules Hello, I own a AstraZeneca Pharmaceuticals LP recalls Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP that is covered by recall D-0585-2018 from AstraZeneca Pharmaceuticals 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.
