FDA recall record

PACLITAXEL INJECTION, USP (semisynthetic) recall — FDA D-016-2014

Labeling: Incorrect or Missing Package Insert- Missing text on the product insert in the "Clinical Studies" and "Specific Adverse Events" sections.

Class IIIclassification
D-016-2014official record ID
Dec 4, 2013report date

Recall record at a glance

Official recordD-016-2014
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmFresenius Kabi USA, LLC
Report dateDec 4, 2013
Recall initiation dateNov 8, 2013
Quantity71,129 vials
LocationLake Zurich, IL, United States

Official product description

PACLITAXEL INJECTION, USP (semisynthetic); 300 mg/50 mL; (6 mg/mL); Multiple Dose Vial;(NDC 63323-763-50); Rx Only; Manufactured for APP Pharmaceuticals, LLC; Schaumburg, IL 60173; Made in India

Why the product was recalled

Labeling: Incorrect or Missing Package Insert- Missing text on the product insert in the "Clinical Studies" and "Specific Adverse Events" sections.

Distribution information

US: Nationwide and Puerto Rico

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

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