FDA recall record

AstraZeneca Pharmaceuticals Lynparza (olaparib) capsules 50 mg, 112 count bottles recall — FDA D-0585-2018

Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).

Class IIIclassification
D-0585-2018official record ID
Mar 14, 2018report date

Recall record at a glance

Official recordD-0585-2018
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAstraZeneca Pharmaceuticals LP
Report dateMar 14, 2018
Recall initiation dateFeb 23, 2018
Quantity18056 bottles
LocationWilmington, DE, United States

Official product description

Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58

Why the product was recalled

Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.