Hospira Inc. recalls Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx
Recalled September 23, 2015 · FDA recall D-0418-2015 · Hospira
Hazard
Defective Container: There were customer complaints of cracked and leaking glass vials. · FDA Class II
Units
83,320 vials
Sold at
Nationwide
Description
Defective Container: There were customer complaints of cracked and leaking glass vials.
Product
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
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →