Hospira Inc. recalls Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx…

Recall date

August 20, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0418-2015

FDA classification

Class II

Brand / firm

Hospira Inc.

Sold / distributed

Nationwide

Why it was recalled

Defective Container: There were customer complaints of cracked and leaking glass vials.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05