FDAApril 27, 2018drug

Docetaxel injection concentrate, 20 mg/mL, 1 mL vial, Rx only, Winthrop U.S. a business of Sanofi-Aventis U.S. LLC., NDC 0955-1020-01

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Superpotent drug: over-concentrated vials of Docetaxel injection concentrate 20 mg/mL may have been distributed.

What to do

FDA enforcement status: Terminated

Brands named

sanofi aventis u ssanofisanofi aventis

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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