FDAOctober 6, 2014drug

Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4332-01.

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

The hazard

Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

What to do

FDA enforcement status: Terminated

Brands named

hospira

Recall history

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

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