FDA-Drug2016-12-14Class III
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
Hospira Inc.
Hazard
Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.
Sold states
US and Puerto Rico
Affected count
287,200 2 mL ampules
Manufactured in
275 N Field Dr, N/A, Lake Forest, IL, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0169-2017Don't want to check this manually?
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