Hospira Inc. recalls 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia…

Recall date

June 29, 2016

Source

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

Recall number

D-0169-2017

FDA classification

Class III

Brand / firm

Hospira Inc.

Sold / distributed

US and Puerto Rico

Why it was recalled

Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01