FDAAugust 28, 2018drug

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 USA. NDC: 0409-1140-01

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

The hazard

Failed Impurities/Degradation Specifications; Out of specification stability testing results at the 18 month time point

What to do

FDA enforcement status: Terminated

Brands named

pfizer

Recall history

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

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Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 USA. NDC: 0409-1140-01 — Recall Details · AllClear