FDADecember 5, 2017drug

Enoxaparin Sodium, Injection 120 mg/0.8 mL, pre-filled, packaged in 10-count cartons, Rx Only, Winthrop US., a business of Sanofi-aventis, U.S. LLC Bridgewater, NJ 08807, NDC 0955-1012-10

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

The hazard

Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL

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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