FDAAugust 20, 2015drug

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

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

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

hospira

UPCs

00409205105

Recall history

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

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